WhoIs globalrxdeals.com

Drug Enforcement Agency

United States of America

The Ryan Haight Act Known as
Online Pharmacy Consumer Protection Act of 2008
Sec. 2. Requirement of a valid prescription for
controlled substances dispensed by means of the Internet.

Who's Behind These Online Pharmacies 

SUMMARY: The Ryan Haight Online Pharmacy Consumer Protection Act,
which was enacted on October 15, 2008,amended the Controlled Substances Act and Controlled Substances Import and Export Act by adding several new provisions to prevent the illegal distribution and dispensing of controlled substances by means of the Internet.
_________________________________

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The following A records are set to 5.199.168.224:

  • 247pillshop.com
  • globalrxdeals.com
  • inter-meds.com
  • ns2.punkman.net
  • premiumrxpills.com

Address lookup
canonical name premiumrxpills.com

aliases
addresses: 5.199.168.224
Domain Whois record

Queried whois.internic.net with “dom premiumrxpills.com

Domain Name: PREMIUMRXPILLS.COM
Registrar: ONLINENIC, INC.
Whois Server: whois.onlinenic.com
Referral URL: http://www.OnlineNIC.com

Name Server: NS1.PUNKMAN.NET
Name Server: NS2.PUNKMAN.NET
Status: clientTransferProhibited
Updated Date: 09-oct-2013
Creation Date: 08-oct-2013
Expiration Date: 08-oct-2014

Last update of whois database: Sun, 22 Dec 2013 19:16:11 UTC
Queried whois.onlinenic.com with “premiumrxpills.com

Domain Name:premiumrxpills.com
Record created:10/8/2013
Record expired:10/08/2014

Domain servers in listed order:
ns1.punkman.net
ns2.punkman.net

WhoIs ~ medonlinepills.com

Drug Enforcement Agency

United States of America

The Ryan Haight Act Known as
Online Pharmacy Consumer Protection Act of 2008
Sec. 2. Requirement of a valid prescription for
controlled substances dispensed by means of the Internet.

Who's Behind These Online Pharmacies 

SUMMARY: The Ryan Haight Online Pharmacy Consumer Protection Act,
which was enacted on October 15, 2008,amended the Controlled Substances Act and Controlled Substances Import and Export Act by adding several new provisions to prevent the illegal distribution and dispensing of controlled substances by means of the Internet.
_________________________________

Toll Free (US):800-532-4808
Toll Free (US):(800)532-4808
Regular US:718-313-1498
Regular US:(718)313-1498
UK:44-203-0110241

Eve Pharmacy
183 North Hampshire Road
New York, NY 10048
Phone:(800) 532-4808
Website: ww.evepharmacy.com

Domain Whois record
Queried whois.internic.net with “dom medonlinepills.com”…

Domain Name: MEDONLINEPILLS.COM
Registrar: EVOPLUS LTD
Whois Server: whois.evonames.com
Referral URL: http://www.evonames.com
Name Server: NS3.IPHOSTER.NET
Name Server: NS4.IPHOSTER.NET
Status: ok
Updated Date: 13-aug-2013
Creation Date: 13-aug-2013
Expiration Date: 13-aug-2014

>>> Last update of whois database: Mon, 23 Sep 2013 14:34:42 UTC <<<
medonline

labex-palm.com

Drug Enforcement Agency

United States of America

The Ryan Haight Act Known as
Online Pharmacy Consumer Protection Act of 2008
Sec. 2. Requirement of a valid prescription for
controlled substances dispensed by means of the Internet.

Who's Behind These Online Pharmacy 

SUMMARY: The Ryan Haight Online Pharmacy Consumer Protection Act,
which was enacted on October 15, 2008,amended the Controlled Substances Act and Controlled Substances Import and Export Act by adding several new provisions to prevent the illegal distribution and dispensing of controlled substances by means of the Internet.
_____________________________________

labex-palm.com highjack ~ used for pharmacy spamming

labex-palmdotcom

labex-palmdotcom2

canadianpharmacyonlinez.com

Buying Prescription Drugs Online May Be Dangerous Says
Drug Enforcement Administration

DEA Logo - Buying Proscription Drugs

National Association of Boards of Pharmacy (NABP)
Warning

The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Who's Behind Online Pharmacy 

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.

Before making a purchase that can affect your health, we strongly recommend that you consult your physician & DO NOT self-medicate.

Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.


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MyRxAffiliateProgram
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evapharmacy.ru
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Rx-Partners
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MyRxPartner
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evapharmacy.ru
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PharmacyExpress
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evapharmacy.ru
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Rx-Partners
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MyRxAffiliateProgram
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MyRxAffiliateProgram/td>
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Everest Network
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evapharmacy.ru
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RxProfits
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MyRxPartner
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evapharmacy.ru
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Source: Legitscript.com

whoIs jium.ru – thepharmacycare.com

Buying Prescription Drugs Online May Be Dangerous Says
Drug Enforcement Administration
Scam Alert 1

DEA Logo - Buying Proscription Drugs

National Association of Boards of Pharmacy (NABP)
Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Who's Behind Online Pharmacy 

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.


Buy Cialis Without Prescription! Buy Cialis Online Without Prescription! Lowest Prices and Satisfaction Guaranteed! Generic and brand drugs with 100% satisfaction guaranteed. Bonus 4-12 pills per order http://jium.ru

Address lookup
canonical name jium.ru.
aliases
addresses 91.240.165.50
Domain Whois record

Queried whois.ripn.net with “jium.ru”…

By submitting a query to RIPN’s Whois Service you agree to abide by the following terms of use:
http://www.ripn.net/about/servpol.html#3.2 (in Russian)
http://www.ripn.net/about/en/servpol.html#3.2 (in English).

domain: JIUM.RU
nserver: ns1.jium.ru. 91.226.116.66
nserver: ns2.jium.ru. 61.150.109.186
state: REGISTERED, DELEGATED, VERIFIED
person: Private Person
registrar: NAUNET-REG-RIPN
admin-contact: https://client.naunet.ru/c/whoiscontact
created: 2012.05.25
paid-till: 2013.05.25
free-date: 2013.06.25
source: TCI

Last updated on 2012.08.16 17:46:39 MSK
Network Whois record

Queried whois.ripe.net with “-B 91.240.165.50
Information related to ‘91.240.165.0 – 91.240.165.255’

inetnum: 91.240.165.0 – 91.240.165.255
netname: Aiming-Invest-sro-net
descr: Aiming Invest s.r.o.
country: CZ
org: ORG-AIs22-RIPE
admin-c: DJ1955-RIPE
tech-c: DJ1955-RIPE
status: ASSIGNED PI
mnt-by: RIPE-NCC-END-MNT
mnt-lower: RIPE-NCC-END-MNT
mnt-by: LeadertelecomBV-mnt
mnt-routes: LeadertelecomBV-mnt
mnt-routes: BECOLINK-MNT
mnt-domains: LeadertelecomBV-mnt
notify: info@leadertelecom.nl
remarks: FOR ABUSE noc@aiminginvest.com
changed: hostmaster@ripe.net 20120629
source: RIPE

organisation: ORG-AIs22-RIPE
org-name: Aiming Invest s.r.o.
org-type: other
address: Nerudova 1840, 530 02 Pardubice, Czech Republic
e-mail: sales@aiminginvest.com
mnt-ref: lidertelecom-mnt
mnt-by: lidertelecom-mnt
changed: info@leadertelecom.ru 20120528
source: RIPE

person: Dante Jimenez
address: Nerudova 1840 Pardubice Czech Republic
phone: +420 725 988 484
e-mail: noc@aiminginvest.com
nic-hdl: DJ1955-RIPE
mnt-by: lidertelecom-mnt
changed: info@leadertelecom.ru 20120528
source: RIPE

Information related to ‘91.240.165.0/24AS199023’

route: 91.240.165.0/24
descr: Aiming Invest s.r.o.
origin: AS199023
mnt-by: BECOLINK-MNT
changed: brazda@omegaplus.cz 20120720
source: RIPE

This query was served by the RIPE Database Query Service version 1.19.5 (WHOIS1)

DNS records

DNS query for 50.165.240.91.in-addr.arpa returned an error from the server: NameError
name class type data time to live
jium.ru IN SOA
server: ns1.jium.ru
email: admin@jium.ru
serial: 2009000000
refresh: 600
retry: 900
expire: 1209600
minimum ttl: 43200
600s (00:10:00)
jium.ru IN NS ns1.jium.ru 600s (00:10:00)
jium.ru IN NS ns2.jium.ru 600s (00:10:00)
jium.ru IN MX
preference: 10
exchange: mail.jium.ru
600s (00:10:00)
jium.ru IN A 91.240.165.50 600s (00:10:00)

— end —

The following A records are set to 91.226.116.66:

ns1.canadamastersdegree.com
ns1.themedprescription.com
ns1.themedsdrugstore.com
ns1.thepharmacycare.com
ns1.thetabletcanada.com
ns1.v60med.com
ns1.viagraciali.net
ns2.abuseprescription.com
ns2.androidtabletdiet.com
ns2.aronelnesslevitra.com
ns2.arontrapill.com
ns2.beastslnessherbal.com
ns2.biolmedsmed.com
ns2.bpgenericspills.com
ns2.freedietrx.net

Canadian Super Store – canada-express-mall.com

Drug Enforcement Agency

United States of America


The Ryan Haight Act Known as
Online Pharmacy Consumer Protection Act of 2008
Sec. 2. Requirement of a valid prescription for
controlled substances dispensed by means of the Internet.

SUMMARY: The Ryan Haight Online Pharmacy Consumer Protection Act,
which was enacted on October 15, 2008,amended the Controlled Substances Act and Controlled Substances Import and Export Act by adding several new provisions to prevent the illegal distribution and dispensing of controlled substances by means of the Internet.


DEA Warning–Buying drugs online may be illegal and dangerous!

Federal law prohibits buying controlled substances such as narcotic pain relievers (e.g., OxyContin®, Vicodin®), sedatives (e.g., Valium®, Xanax®, Ambien®), stimulants (e.g., phentermine, phendimetrazine, Adderall®, Ritalin®) and anabolic steroids (e.g., Winstrol®, Equipoise®) without a valid prescription from your doctor.

This means there must be a real doctor-patient relationship, which by most state laws requires a physical examination. Prescriptions written by “cyber doctors” relying on online questionnaires are not legitimate under the law.



Address lookup
canonical name canada-express-mall.com

aliases
addresses 93.158.114.136
Domain Whois record

Queried whois.internic.net with “dom canada-express-mall.com”…

Domain Name: CANADA-EXPRESS-MALL.COM
Registrar: NANJING IMPERIOSUS TECHNOLOGY CO. LTD.
Whois Server: whois.communigal.net
Referral URL: http://www.DomainersChoice.com
Name Server: NS10.DNSMADEEASY.COM
Name Server: NS11.DNSMADEEASY.COM
Name Server: NS12.DNSMADEEASY.COM
Name Server: NS13.DNSMADEEASY.COM
Name Server: NS14.DNSMADEEASY.COM
Name Server: NS15.DNSMADEEASY.COM
Status: clientTransferProhibited
Updated Date: 03-jul-2012
Creation Date: 18-oct-2011
Expiration Date: 18-oct-2013

Last update of whois database: Sun, 12 Aug 2012 16:15:50 UTC
Queried whois.communigal.net with “canada-express-mall.com
canada-express-mall.com

Registrant Contact Information :
Private
Registration
WhoisGuardService.com
canada-express-mall.com@dnwhoisguard.com
Tian Hong Shan Zhuang, BLd. 7, Office 104
Nanjing
210049
86 2584752362
86 2584752360

Admin Contact Information :
Private
Registration
WhoisGuardService.com
canada-express-mall.com@dnwhoisguard.com
Tian Hong Shan Zhuang, BLd. 7, Office 104
Nanjing
210049
86 2584752362
86 2584752360

Tech Contact Information :
Private
Registration
WhoisGuardService.com
canada-express-mall.com@dnwhoisguard.com
Tian Hong Shan Zhuang, BLd. 7, Office 104
Nanjing
210049
86 2584752362
86 2584752360

Billing Contact Information :
Private
Registration
WhoisGuardService.com
canada-express-mall.com@dnwhoisguard.com
Tian Hong Shan Zhuang, BLd. 7, Office 104
Nanjing
210049
86 2584752362
86 2584752360

Name Server : NS10.DNSMADEEASY.COM
Name Server : NS15.DNSMADEEASY.COM
Name Server :

Creation date : 2011-10-18/05:45:39
Updated date : 2012-07-03/14:45:00
Expiration date : 2013-10-18/05:45:39

Status : clientTransferProhibited

Network Whois record

Queried whois.ripe.net with “-B 93.158.114.136
Information related to ‘93.158.114.0 – 93.158.114.255’

inetnum: 93.158.114.0 – 93.158.114.255
netname: SWEDENDEDICATED-NET
descr: Sweden Dedicated
remarks: Abuse: abuse@itproductions.se
country: SE
admin-c: PORT80-RIPE
tech-c: PORT80-RIPE
status: ASSIGNED PA
notify: ripemodifications@port80.se
mnt-by: PORT80-MNT
changed: registry@port80.se 20090309
changed: registry@port80.se 20091202
source: RIPE

role: Port80 Staff
address: Phonera Networks AB
address: Hammarby Fabriksvag 25
address: 120 33 Stockholm
address: Sweden
phone: +46 8 5000 3000
fax-no: +46 8 5000 3010
abuse-mailbox: abuse@abuse.phonera.se
remarks: ********************************
remarks: Abuse related issues is reported
remarks: to abuse@abuse.phonera.se
remarks: ********************************
e-mail: abuse@abuse.phonera.se
e-mail: noc@p80.net
e-mail: registry@port80.se
admin-c: RC765-RIPE
tech-c: RC765-RIPE
nic-hdl: PORT80-RIPE
mnt-by: PORT80-MNT
changed: registry@port80.se 20001115
changed: registry@port80.se 20081020
changed: registry@port80.se 20100529
source: RIPE

Information related to ‘93.158.64.0/18AS39369’

route: 93.158.64.0/18
descr: Port80, Pan European Network
origin: AS39369
mnt-by: PORT80-MNT
changed: registry@port80.se 20090821
source: RIPE
notify: ripemodifications@port80.se

This query was served by the RIPE Database Query Service version 1.19.5 (WHOIS1)

DNS records

DNS query for 136.114.158.93.in-addr.arpa returned an error from the server: NameError
name class type data time to live
canada-express-mall.com IN SOA
server: ns10.dnsmadeeasy.com
email: dns@dnsmadeeasy.com
serial: 2009010105
refresh: 43200
retry: 3600
expire: 1209600
minimum ttl: 180
86400s (1.00:00:00)
canada-express-mall.com IN NS ns12.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN NS ns11.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN NS ns10.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN NS ns14.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN NS ns13.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN NS ns15.dnsmadeeasy.com 86400s (1.00:00:00)
canada-express-mall.com IN A 93.158.114.136 120s (00:02:00)
canada-express-mall.com IN MX
preference: 10
exchange: mail.canada-express-mall.com
120s (00:02:00)

— end —

4Rx .com ~ 4Rx.net

Buying Prescription Drugs Online May Be Dangerous Says
Drug Enforcement Administration
Scam Alert 1

DEA Logo - Buying Proscription Drugs

National Association of Boards of Pharmacy (NABP)
Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Who's Behind Online Pharmacy 

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.


4rx.com4rx.com fraudulent website Internet

4rx.com
Phone:
secure.4rx.com/index.html
Internet,
India

RX is selling ed drugs with a cut down amount of the actual advertised ingredients.They advertise sidenafil citrate 100mg pills however they supply about 5mg.

I believe they buy name brand sidenafil citrate 100mg and cut it down and make their own pills in India and ship from Hong Kong. They also do this with Tadalafil and Vardenafil HCL.

The reason I know this is I have a true ED and have tried the name brand drugs at different doses and can gage through experience.

These fraudulent pills do not do the trick….. speaking from experience.

Just would like to warn others.

a short cut to the website http://secure.4rx.com/index.html

Kind Regards,
Ric
city
Australia

Source: Ripoffreport

Related Domains

  1. 4Rx.com http://piils.com
  2. 4Rx.com http://4rxpharm.com
  3. 4Rx.com http://www.4rx.name
  4. 4Rx.com www-4rx.com
  5. 4Rx.com http://buysildenafilcitrate.info
  6. 4Rx.com http://viagrasexdrug.com
  7. 4Rx.com http://www.worldexpressrx.com
  8. 4Rx.com http://www.4rx.com
  9. 4Rx.net http://www.4rx.net

4Rx

Address lookup

canonical name www.4rx.com.
aliases
addresses 174.142.47.58

Domain Whois record

Queried whois.internic.net with “dom 4rx.com“…

   Domain Name: 4RX.COM
   Registrar: NAMESCOUT CORP
   Whois Server: whois.namescout.com
   Referral URL: http://www.namescout.com
   Name Server: NS2.BLOCKDOS.NET
   Name Server: NS3.BLOCKDOS.NET
   Name Server: NS5.BLOCKDOS.NET
   Status: ok
   Updated Date: 28-oct-2008
   Creation Date: 25-nov-2003
   Expiration Date: 25-nov-2009

>>> Last update of whois database: Mon, 22 Jun 2009 09:46:16 UTC <<<

Queried whois.namescout.com with “4rx.com“…

The results below are provided by Namescout.com.
(whois.Namescout.com)

Domain: 4rx.com

  Date Registered: 10/28/08
    Date Modified: 10/29/08
      Expiry Date: 11/25/09
      	     DNS1: NS2.BLOCKDOS.NET
      	     DNS2: NS3.BLOCKDOS.NET

  Registrant

                   4RX
                   Victor Gonzalez
                   451 Calle Herrera Toro. Qta. Bubu
                   Caracas, -- (BS)
                   00000

  Administrative Contact

                   4RX
                   Victor Gonzalez
                   451 Calle Herrera Toro. Qta. Bubu
                   Caracas,  (VE)
                   00000
                   webmaster@4rx.com
                   (877)728-9479

  Technical Contact

                   4RX
                   Victor Gonzalez
                   451 Calle Herrera Toro. Qta. Bubu
                   Caracas,  (VE)
                   00000
                   webmaster@4rx.com
                   (877)728-9479

        Registrar: Namescout.com

Register your domain now at www.Namescout.com

Network Whois record

Queried whois.arin.net with “174.142.47.58“…

OrgName:    iWeb Technologies Inc.
OrgID:      GIT-20
Address:    20, place du Commerce
City:       Montreal
StateProv:  QC
PostalCode: H3E-1Z6
Country:    CA

NetRange:   174.142.0.0 - 174.142.255.255
CIDR:       174.142.0.0/16
OriginAS:   AS32613
NetName:    IWEB-BLK-06
NetHandle:  NET-174-142-0-0-1
Parent:     NET-174-0-0-0-0
NetType:    Direct Allocation
NameServer: NS1.IWEB-HOSTING.COM
NameServer: NS2.IWEB-HOSTING.COM
Comment:
RegDate:    2008-12-19
Updated:    2008-12-19

OrgAbuseHandle: ABUSE1906-ARIN
OrgAbuseName:   Abuse Coordinator
OrgAbusePhone:  +1-514-286-4242
OrgAbuseEmail:  abuse@noc.privatedns.com

OrgNOCHandle: NETWO2356-ARIN
OrgNOCName:   Network Administrator
OrgNOCPhone:  +1-514-286-4242
OrgNOCEmail:  net-admin@noc.privatedns.com

OrgTechHandle: NETWO2356-ARIN
OrgTechName:   Network Administrator
OrgTechPhone:  +1-514-286-4242
OrgTechEmail:  net-admin@noc.privatedns.com

# ARIN WHOIS database, last updated 2009-06-21 20:00

DNS records

name class type data time to live
http://www.4rx.com IN A 174.142.47.58 120s (00:02:00)
4rx.com IN SOA
server: ns2.blockdos.net
email: support.server4sale.com
serial: 2008100601
refresh: 86400
retry: 7200
expire: 3600000
minimum ttl: 86400
86400s (1.00:00:00)
4rx.com IN NS ns2.blockdos.net 86400s (1.00:00:00)
4rx.com IN NS ns3.blockdos.net 86400s (1.00:00:00)
4rx.com IN NS ns5.blockdos.net 86400s (1.00:00:00)
4rx.com IN MX
preference: 5
exchange: mail.4rx.com
120s (00:02:00)
4rx.com IN MX
preference: 10
exchange: 4rx.com
120s (00:02:00)
4rx.com IN A 174.142.47.58 120s (00:02:00)
58.47.142.174.in-addr.arpa IN PTR ip-174-142-47-58.static.privatedns.com 3600s (01:00:00)

— end —

perfectbreastsnow.com – Colocationamerica.com

Buying Prescription Drugs Online May Be Dangerous Says
Drug Enforcement Administration
Scam Alert 1

DEA Logo - Buying Proscription Drugs

National Association of Boards of Pharmacy (NABP)
Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Who's Behind Online Pharmacy 

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.



Boussant Breast enlargement pills are one of the top rated breast enhancement products and safest on the market. It’s one the most affordable natural breast enlargement products that’s designed to increase size, shape and firmness of a woman’s breasts in just a couple of weeks guaranteed.

Address lookup
canonical name http://www.perfectbreastsnow.com

aliases
addresses 208.70.252.238
Domain Whois record

Queried whois.internic.net with “dom perfectbreastsnow.com”…

Domain Name: PERFECTBREASTSNOW.COM
Registrar: GODADDY.COM, INC.
Whois Server: whois.godaddy.com
Referral URL: http://registrar.godaddy.com
Name Server: NS1.26DNS.COM
Name Server: NS2.26DNS.COM
Status: clientDeleteProhibited
Status: clientRenewProhibited
Status: clientTransferProhibited
Status: clientUpdateProhibited
Updated Date: 12-jul-2010
Creation Date: 07-jul-2003
Expiration Date: 10-oct-2012

Last update of whois database: Fri, 25 Nov 2011 06:31:13 UTC
Queried whois.godaddy.com with “perfectbreastsnow.com

Registrant:
Colocation
9360 W. Flamingo Rd.
Suite 110-178
Las Vegas, Nevada 89147
United States

Registered through: GoDaddy.com, Inc. (http://www.godaddy.com)
Domain Name: PERFECTBREASTSNOW.COM
Created on: 07-Jul-03
Expires on: 10-Oct-12
Last Updated on: 12-Jul-10

Administrative Contact:
America, Colocation Support@ColocationAmerica.com
Colocation
9360 W. Flamingo Rd.
Suite 110-178
Las Vegas, Nevada 89147
United States
+1.8002968915 Fax —

Technical Contact:
America, Colocation Support@ColocationAmerica.com
Colocation
9360 W. Flamingo Rd.
Suite 110-178
Las Vegas, Nevada 89147
United States
+1.8002968915 Fax —

Domain servers in listed order:
NS1.26DNS.COM
NS2.26DNS.COM
Network Whois record

Queried whois.arin.net with “n 208.70.252.238″…

NetRange: 208.70.248.0 – 208.70.255.255
CIDR: 208.70.248.0/21
OriginAS: AS21769
NetName: CAC-BLOCK1
NetHandle: NET-208-70-248-0-1
Parent: NET-208-0-0-0-0
NetType: Direct Allocation
RegDate: 2006-10-03
Updated: 2007-09-20
Ref: http://whois.arin.net/rest/net/NET-208-70-248-0-1

OrgName: Colocation America Corporation
OrgId: CAC-89
Address: 9360 W Flamingo Rd Suite 110-178
City: Las Vegas
StateProv: NV
PostalCode: 89147
Country: US
RegDate: 2005-04-06
Updated: 2008-11-25
Ref: http://whois.arin.net/rest/org/CAC-89

OrgTechHandle: NOC1792-ARIN
OrgTechName: Network Operations Center
OrgTechPhone: +1-800-296-8915
OrgTechEmail: noc@colocationamerica.com
OrgTechRef: http://whois.arin.net/rest/poc/NOC1792-ARIN

OrgNOCHandle: NOC1792-ARIN
OrgNOCName: Network Operations Center
OrgNOCPhone: +1-800-296-8915
OrgNOCEmail: noc@colocationamerica.com
OrgNOCRef: http://whois.arin.net/rest/poc/NOC1792-ARIN

OrgAbuseHandle: ABUSE1755-ARIN
OrgAbuseName: Abuse Department
OrgAbusePhone: +1-800-296-8915
OrgAbuseEmail: abuse@colocationamerica.com
OrgAbuseRef: http://whois.arin.net/rest/poc/ABUSE1755-ARIN

RNOCHandle: NOC1792-ARIN
RNOCName: Network Operations Center
RNOCPhone: +1-800-296-8915
RNOCEmail: noc@colocationamerica.com
RNOCRef: http://whois.arin.net/rest/poc/NOC1792-ARIN

RTechHandle: NOC1792-ARIN
RTechName: Network Operations Center
RTechPhone: +1-800-296-8915
RTechEmail: noc@colocationamerica.com
RTechRef: http://whois.arin.net/rest/poc/NOC1792-ARIN

RAbuseHandle: ABUSE1755-ARIN
RAbuseName: Abuse Department
RAbusePhone: +1-800-296-8915
RAbuseEmail: abuse@colocationamerica.com
RAbuseRef: http://whois.arin.net/rest/poc/ABUSE1755-ARIN
DNS records

name class type data time to live
http://www.perfectbreastsnow.com IN A 208.70.252.238 14400s (04:00:00)
perfectbreastsnow.com IN MX
preference: 10
exchange: mail.perfectbreastsnow.com
600s (00:10:00)
perfectbreastsnow.com IN TXT v=spf1 ip4:208.70.253.18 a mx ip4:208.70.248.18 ~all 600s (00:10:00)
perfectbreastsnow.com IN A 208.70.252.238 14400s (04:00:00)
perfectbreastsnow.com IN SOA
server: ns1.26dns.com
email: corp.multacom.com
serial: 2011091904
refresh: 7200
retry: 3600
expire: 1209600
minimum ttl: 600
600s (00:10:00)
perfectbreastsnow.com IN NS ns1.26dns.com 86400s (1.00:00:00)
perfectbreastsnow.com IN NS ns2.26dns.com 86400s (1.00:00:00)
238.252.70.208.in-addr.arpa IN PTR 208.70.252.238-unallocated.colocationamerica.com 7200s (02:00:00)
— end —

WhoIs rx-s.net/

Buying Prescription Drugs Online Scam Alert 1
May Be Dangerous
Says Drug Enforcement Administration



DEA Logo - Buying Proscription Drugs

Click Here
National Association of Boards of Pharmacy (NABP)

Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Behind The Online Pharmacy

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medicines Over the Internet

FDA – Consumer Safety Guide

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.

Department of Justice – Ryan Haight Act
Read More Health Canada

For a prescription to be valid under federal and state law, there must be a bona fide doctor patient relationship, which is defined by most state laws to require a physical examination. “Completing a questionnaire that is then reviewed by a doctor hired by the internet pharmacy could not be considered the basis for a doctor/patient relationship.” Vol. 66 Federal Register 82, PP 21181-21184 (April 27, 2001)

Moreover, if the prescription drug is a controlled substance and the drug is being imported into the U.S. from a foreign country and being shipped to anyone other than a DEA-registered importer, such transaction is a felony in violation of Sections 957 and 960 of Title 21, United States Code.


Address lookup
canonical name rx-s.net.

aliases
addresses 69.65.98.191
Domain Whois record

Queried whois.internic.net with “dom rx-s.net”…

Domain Name: RX-S.NET
Registrar: INTERNET.BS CORP.
Whois Server: whois.internet.bs
Referral URL: http://www.internet.bs
Name Server: NS1.RX-S.NET
Name Server: NS2.RX-S.NET
Status: clientTransferProhibited
Updated Date: 23-oct-2010
Creation Date: 07-sep-2004
Expiration Date: 07-sep-2012

Last update of whois database: Sun, 20 Mar 2011 21:24:07 UTC <<<

Queried whois.internet.bs with "rx-s.net
Domain rx-s.net

Date Registered: 2004-9-7
Date Modified: 2010-10-23
Expiry Date: 2012-9-7

DNS1: ns1.rx-s.net
DNS2: ns2.rx-s.net

Registrant
Private Whois Service
Private Whois Service ipworfu4cc283719efd5@qc8iazv4cbecce2a1df1.privatewhois.net
*******PLEASE DO NOT SEND LETTERS******
****Contact the owner by email only****
c/o rx-s.net
N4892 Nassau
Bahamas

Administrative Contact
Private Whois Service
Private Whois Service aid1mds4cc28371aa761@qc8iazv4cbecce2a1df1.privatewhois.net
*******PLEASE DO NOT SEND LETTERS******
****Contact the owner by email only****
c/o rx-s.net
N4892 Nassau
Bahamas
Tel: +852.81720004

Technical Contact
Private Whois Service
Private Whois Service un3wc7a4cc28371a68e6@qc8iazv4cbecce2a1df1.privatewhois.net
*******PLEASE DO NOT SEND LETTERS******
****Contact the owner by email only****
c/o rx-s.net
N4892 Nassau
Bahamas
Tel: +852.81720004

Registrar: Internet.bs Corp.
Registrar's Website : http://www.internetbs.net/

Network Whois record

Whois query for 69.65.98.191 failed: TimedOut

Queried whois.arin.net with “n 69.65.98.191″…

NetRange: 69.65.96.0 – 69.65.127.255
CIDR: 69.65.96.0/19
OriginAS: AS30568, AS11434, AS14383
NetName: VCS-NET-1
NetHandle: NET-69-65-96-0-1
Parent: NET-69-0-0-0-0
NetType: Direct Allocation
RegDate: 2006-02-06
Updated: 2009-08-13
Ref: http://whois.arin.net/rest/net/NET-69-65-96-0-1

OrgName: Virtacore Systems Inc
OrgId: VIRTA
Address: 44470 Chilum Place
City: Ashburn
StateProv: VA
PostalCode: 20147
Country: US
RegDate: 2009-07-01
Updated: 2009-07-01
Ref: http://whois.arin.net/rest/org/VIRTA

ReferralServer: rwhois://rwhois.virtacore.com:4321

OrgAbuseHandle: ABUSE2329-ARIN
OrgAbuseName: Abuse Department
OrgAbusePhone: +1-703-621-3565
OrgAbuseEmail: abuse@virtacore.com
OrgAbuseRef: http://whois.arin.net/rest/poc/ABUSE2329-ARIN

OrgTechHandle: NETWO3166-ARIN
OrgTechName: Network Operations
OrgTechPhone: +1-703-621-3565
OrgTechEmail: noc@virtacore.com
OrgTechRef: http://whois.arin.net/rest/poc/NETWO3166-ARIN

OrgNOCHandle: NETWO3166-ARIN
OrgNOCName: Network Operations
OrgNOCPhone: +1-703-621-3565
OrgNOCEmail: noc@virtacore.com
OrgNOCRef: http://whois.arin.net/rest/poc/NETWO3166-ARIN

DNS records
name class type data time to live
rx-s.net IN MX
preference: 10
exchange: aspmx.l.google.com
14400s (04:00:00)
rx-s.net IN MX
preference: 20
exchange: alt1.aspmx.l.google.com
14400s (04:00:00)
rx-s.net IN MX
preference: 20
exchange: alt2.aspmx.l.google.com
14400s (04:00:00)
rx-s.net IN MX
preference: 30
exchange: aspmx2.googlemail.com
14400s (04:00:00)
rx-s.net IN MX
preference: 30
exchange: aspmx3.googlemail.com
14400s (04:00:00)
rx-s.net IN MX
preference: 30
exchange: aspmx4.googlemail.com
14400s (04:00:00)
rx-s.net IN MX
preference: 30
exchange: aspmx5.googlemail.com
14400s (04:00:00)
rx-s.net IN MX
preference: 0
exchange: rx-s.net
14400s (04:00:00)
rx-s.net IN SOA
server: ns1.rx-s.net
email: alexo.pisem.net
serial: 2008122401
refresh: 86400
retry: 7200
expire: 3600000
minimum ttl: 86400
86400s (1.00:00:00)
rx-s.net IN NS ns1.rx-s.net 86400s (1.00:00:00)
rx-s.net IN NS ns2.rx-s.net 86400s (1.00:00:00)
rx-s.net IN A 69.65.98.191 14400s (04:00:00)
191.98.65.69.in-addr.arpa IN PTR unknown191.98.65.69.defenderhosting.com 10800s (03:00:00)

— end —


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FDA Warning – Rx-promotion

October 12, 2010
UNITED STATES DEPARTMENT OF HEALTH AND HUMAN SERVICES

FOOD AND DRUG ADMINISTRATION
ROCKVILLE, MD 20903

TO: support@rx-drugs-support.com
FROM: Food and Drug Administration Internet Pharmacy Task Force
RE: Internet Marketing of Unapproved and Misbranded Drugs
DATE: October 8, 2010

WARNING LETTER

The United States Food and Drug Administration (FDA) recently reviewed your websites (listed in the table located at the bottom of this letter) and has determined that your websites offer products for sale in violation of the Federal Food, Drug, and Cosmetic Act (FFDCA). More specifically, the websites listed below offer unapproved and misbranded new drugs for sale in violation of sections 301(a), 301(d), and 505(a) of the FFDCA [21 U.S.C. §§ 331(a), 331(d), and 355(a)]. We request that you immediately cease marketing violative drug products to United States consumers.

Unapproved New Drugs

Certain products you offer for sale through your websites are drugs within the meaning of section 201(g) of the FFDCA [21 U.S.C. § 321(g)] because they are intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease and/or because they are intended to affect the structure or function of the body. These products are also new drugs as defined by section 201(p) of the FFDCA [21 USC § 321(p)], because they are not generally recognized as safe and effective for their labeled uses. No approved applications pursuant to section 505 of the FFDCA (21 USC § 355) are in effect for these products. Accordingly, their introduction or delivery for introduction into interstate commerce violates sections 505(a) and 301(d) of the FFDCA [21 USC §§ 355(a) and 331(d)].

As a few examples, your firm offers for sale through your websites “Viagra Professional,” “Cialis Super Active,” “Female Viagra,” “Acomplia,” “Cialis Professional,” and “Viagra Soft.” “Viagra” and “Cialis” are the names of FDA-approved drugs well-known for their intended use(s) to treat disease. Similarly, Acomplia (rimonabant) is well-known as the name of a drug previously approved in the European Union. It has never been approved by FDA, and in June 2007, FDA’s Endocrinologic and Metabolic Drugs Advisory Committee unanimously voted not to recommend approval of the drug because of increased risk of neurological and psychiatric side effects including seizures, depression, anxiety, insomnia, aggressiveness, and suicidal thoughts among patients. Including drug names such as “Viagra,” “Cialis,” and “Acomplia” causes products such as “Viagra Professional,” “Cialis Super Active,” “Female Viagra,” “Acomplia,” “Cialis Professional,” and “Viagra Soft” to be subject to regulation as drugs under Section 201(g) of the FFDCA because they are intended for use in the diagnosis, cure, mitigation treatment, or prevention of disease. As stated above, no approved applications pursuant to section 505 of the FFDCA (21 USC § 355) are in effect for these products. Your offering these products for sale without approved applications violates the FFDCA.

Misbranded Drugs

Your websites offer prescription drugs – some of which include controlled substances, particularly concerning because of their potential for abuse and dependency – for sale without
requiring that the drugs be dispensed only upon a prescription from a practitioner licensed by law to administer such drugs. Therefore, the drugs are misbranded under section 503(b)(1) of the FFDCA [21 U.S.C. § 353(b)(1)].

Additionally, because the above mentioned drugs are intended for conditions that are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners, adequate directions cannot be written for them so that a layman can use these products safely for their intended uses. Consequently, their labeling fails to bear adequate directions for their intended uses, causing them to be misbranded under section 502(f)(1) of the FFDCA [21 U.S.C. § 352(f)(1)]. Because your products, such as “Viagra Professional,” “Cialis Super Active,” “Female Viagra,” “Acomplia,” “Cialis Professional,” and “Viagra Soft,” lack required approved applications, they are not exempt under 21 C.F.R. § 201.115 from the requirements of section 502(f)(1) of the FFDCA.

In addition, your websites offer Accutane (isotretinoin) for sale. Accutane is a potentially dangerous prescription drug that should only be taken under the close supervision of a healthcare professional and pharmacist. Because isotretinoin has serious risks, FDA-approved drugs containing isotretinoin are available in the U.S. only under specially created safety controls. More specifically, among other requirements, patients and their doctors and pharmacists are required by FDA to register with the iPLEDGE program in order to receive this medication. These safety controls are bypassed when this drug is purchased from foreign sources or over the Internet, placing patients who use this drug at risk. The Accutane product offered for sale on your websites is misbranded within the meaning of section 502(f)(1) of the FFDCA [21 U.S.C. § 352(f)(1)] in that labeling for the drug fails to bear adequate directions for use. The introduction or delivery for introduction into interstate commerce of misbranded products violates section 301 of the FFDCA (21 U.S.C. § 331).

* * *

FDA is taking this action against your firm because of the inherent risk in buying unapproved and misbranded new drugs. Unapproved new drugs from unregulated sources do not have the same assurance of safety and effectiveness as drugs subject to FDA oversight and such drugs have been found to be contaminated, counterfeit, contain varying amounts of active ingredients, or contain different ingredients altogether. For drugs that are regulated by FDA, FDA protections include rigorous scientific standards for new drug approval and labeling review for accuracy and completeness, manufacturing procedures and testing performed under closely controlled conditions at FDA-registered and inspected facilities. In addition, pharmacies and wholesalers who sell or distribute prescription drugs in the U.S. are licensed by the states. Unapproved new drugs delivered to the American public from unregulated sources may not be safe and effective.

This letter is not intended to identify all of the ways in which your activities might be in violation of law. It is your responsibility to ensure that all products marketed by your firm are in compliance with the FFDCA and its implementing regulations. You should take prompt action to correct the violations noted above. Failure to correct these violations promptly may result in regulatory action, including but not limited to, seizure and/or injunction without further notice.

Please notify this office in writing within 15 working days of receipt of this letter of any steps you have taken or will take to correct the noted violations and to prevent their recurrence. If the corrective action(s) cannot be completed within 15 working days, state the reason for the delay and the time within which the correction(s) will be completed. Your response should be sent to FDAInternetPharmacyTaskForce-CDER@fda.hhs.gov. Please direct any inquiries concerning this letter to FDA’s Internet Pharmacy Task Force at FDAInternetPharmacyTaskForce-CDER@fda.hhs.gov or (301) 796-3110.

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Sincerely,

/S/
Michael M. Levy, Jr., Esq.
Director
Division of New Drugs and Labeling Compliance
Office of Compliance
Center for Drug Evaluation and Research

cc:
Rx-Promotion
Marianne Knowles
Suite 2, Portland House
Glacis Rd, GI

Alex James
Internet Marketing Pro’s LLC
domain486@gmail.com
3422 Old Capitol Trail
Wilmington, DE 19808-6192

Annette Goldi and Annette Cirino
domain486@gmail.com
Landerbrook Drive
Cleveland, OH 44023

Hardy, Anthony
anthonythardy@aol.com
11306 Kettering Terrace
Largo, MD 20774

Nexton Limited
Ryabov Sergey
director@climbing-games.com
Scherbakova st., 6-38
Saint-Petersburg, 197375
RU

Aiden Aibo
doctoraibo@yahoo.com.au
219 Macquarie Street
Sydney 2000
AU

Brian Tracy
dzz1234567890qwertyuiopfckjff@gmail.com
Baloboo 13-66
NY, 12345
US

Roman Vozhev
50 Let Pobedi, 1/275
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UA

Said Umarik
enot.spec@gmail.com
pl. Mustakillik 5
Tashkent, 700078
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Smartsol Inc.
Jorge Smark
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Strawinskylaan 1221
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Spik Janot
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FDA Warning Letter – Cardio Renew Inc

October 12 2010

WARNING LETTER Refer to MIN 11-01
OVERNIGHT MAIL via UPS

Kevin Raymond
Jay Hoogenakker
Cardio Renew, Inc.
15050 Cedar Avenue, #116-315
Apple Valley, Minnesota 55124

Dear Messrs. Raymond and Hoogenakker:

This is to advise you that the Food and Drug Administration (FDA) has reviewed your websites at the Internet addresses

and has determined that the products “Cardio Renew” and “Cardio Restore” are promoted for conditions that cause the products to be drugs under section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(g)(1)(B)]. The therapeutic claims on your websites establish that the products are drugs because they are intended for use in the cure, mitigation, treatment, or prevention of disease. The marketing of these products with these claims violates the Act.

Examples of some of the claims observed on your websites include:

Cardio Renew (cardiorenew.com. cardio-renew.com. cardiorenew.org):

On the Home pages of http://www.cardiorenew.com and www.cardiorenew.org:
• “EDTA [an ingredient in your product] Chelation Promotes: … Normalized Blood Pressure … Normalized Cholesterol Levels”

Your webpage titled “Benefits of EDTA Chelation Therapy” states, “Cardio Renew is 100% pure liquid EDTA chelation therapy that will … increase[] blood flow…. If your blood flow is restricted due to blockage, your body is not receiving the proper nourishment, which causes poor health conditions. Now, if you reduce the blockage and increase circulation, your body receives the proper blood rich in oxygen and nutrients which can allow it to recuperate, regenerate and operate normally once again.” Below this statement, your webpage discusses many diseases in specific detail. Some of the listed diseases and more specific claims include:

• “Alzheimer’s disease: … In mixed dementia, Alzheimer’s and vascular dementia (reduced blood flow to parts of the brain) occur together. Increasing circulation with liquid chelation therapy brings blood rich in oxygen and nutrients to all parts of the body, increasing energy and alertness.”
• “Angina: Chest pain or discomfort that occurs when the heart does not get enough blood due to build up in the coronary arteries. … Reducing blockage and increasing circulation through EDTA chelation therapy can help the body function closer to normal.”
• “Arteriosclerosis:. ” Reducing blockage and increasing circulation through EDTA chelation therapy, can assure a healthy blood flow with oxygen to the heart.”
• “Atherosclerosis”
• “Bursitis: … Poor circulation can increase inflammation. Increasing circulation through chelation therapy can help the body function closer to normal.”
• “Cardiac Arrhythmia”
• “Cardiovascular Disease”
• “Cholesterol Reduction: … By increasing blood flow by removing mineral deposits and heavy metals from the body; liquid EDTA chelation treatment can assist in reducing blockage in the arteries and veins. Read more about how you can reduce your cholesterol with chelation therapy.”
• “Coronary Artery Disease”
• “Diabetes Mellitus”
• “Diabetic Neuropathy”
• “Diabetic Retinopathy”
• “Elevated Blood Fats (Hyperlipidemia)”
• “Erectile Dysfunction”
• “Fibromyalgia: … There are multiple physiologic abnormalities in someone with FM, including low levels of blood flow to the thalamus region of the brain. Increasing circulation through oral chelation can help the body function closer to normal.”
• “Gangrene”
• “Heart Failure: … Reducing blockage and increasing circulation through chelation therapy, can assure a healthy blood flow with oxygen and nutrients to the heart.”
• “Heavy Metal Poisoning: … EDTA chelation removes heavy metals and excessive minerals from the body, reducing the risk for overload or toxicity.”
• “High Blood Pressure”
• “Intermittent Claudication: The pain is due to insufficient blood flow in the legs (caused by blocked arteries) It is the most prominent symptom of PAD (Peripheral
Artery Disease). Reducing blockage and increasing circulation through oral EDTA chelation, can assure a healthy blood flow throughout the body.”
• “Ischemia: A condition in which the blood flow (and thus oxygen) is restricted to a part of the body…. Reducing blockage and increasing circulation through oral chelation therapy, can assure a healthy blood flow throughout the body.”
• “Macular Degeneration”
• “Multiple Sclerosis”
• “Osteoarthritis: … Poor circulation can increase inflammation…. Increasing circulation through EDTA chelation therapy can help the body function closer to normal.”
• “Parkinson’s Disease”
• “Peyronie’s Disease”
• “Psoriasis”
• “Raynaud’s Disease: … It’s a disorder of the blood vessels that supply blood to the skin, these arteries narrow, limiting circulation to affected areas. Increasing circulation with liquid chelation therapy brings blood rich in oxygen and nutrients to all parts of the body.”
• “Rheumatoid Arthritis: … Because EDTA acts as a good anti-inflammatory, along with the chelation process increasing blood flow, oral chelation therapy can help relieve pains and conditions caused by arthritis.”
• “Scleroderma”
• “Senile Dementia”
• “Strokes: An injury to the brain due to the interruption of the blood supply when an artery becomes blocked, or a blood vessel breaks…. Increasing circulation and reducing blockage with liquid EDTA chelation therapy brings blood rich in oxygen and nutrients to all parts of the body.”
• “Thrombophlebitis: The swelling of a vein caused by a blood clot, due to diminished blood flow…. Reducing blockage and increasing circulation through EDTA chelation therapy can help the body function closer to normal.”
• “Transient Ischemic Attack (TIA): … TIA’s occur when a blood clot temporarily clogs an artery and part of the brain doesn’t get the blood it needs. EDTA chelation reduces the viscosity or ‘stickiness’ of the blood, improving blood circulation throughout the entire body.”

On your webpage titled “Angina Symptoms:”
• “Treatment for Angina and Chelation Therapy … Cardio Renew’s oral liquid EDTA chelation therapy can assist in angina relief.”

On your webpage titled “Hypertension and Blood Pressure:”
• “Chelation therapy from Cardio Renew can help you relieve hypertension…. [R]eturn your blood pressure to a healthy level.”

On your webpage titled “Peripheral Artery Disease (PAD):”
• “Cardio Renew can assist in relieving Peripheral Artery Disease symptoms.”

In addition, your websites

contain disease claims in the form of personal testimonials.

The following are excerpts from a webpage entitled “EDTA Chelation Therapy Testimonials:”

• “I just returned from the doctor after taking this product [Cardio Renew] for two months. I am 58 and for 3 years I’ve had a partially [sic] blocked carotoid left artery and blood pressure hovering between 130 and 150/90. The doctor recently ordered a MRl and MRA which showed NO blockage and my blood pressure was 116170!! The ONLY thing I’ve been doing differently is taking the EDTA.”
• “I was diagnosed with PAD [Peripheral Artery Disease] and was finding it more and more difficult to walk …. I’ve been on Cardio Renew for 3 1/2 weeks now …. I can WALK!!!!!! … I’ve managed to avoid the procedures that the doctors wanted to do on me.”
• “I have been using Cardio Renew for two years after two by-pass operations and just got a clearance from my heart doctor that I will not need a third by-pass… , My arthritis is gone …. It seems that cleaning out all my arteries has given my body a chance to regenerate all organs…. I am now using it for AMD [Age-related Macular Degeneration], the dry type … it should unplug the veins in my eye.”
• “I have been suffering daily severe chest pains [hyperlink to “Angina Symptoms” webpage] and breathing problems. I started your basic Cardio Renew program on August 30, 2008, and am 3 weeks into the program. NO MORE CHEST PAINS AT ALL, my breathing has gotten 200% better …. I am also a diabetic, with severe foot and hand pains and numbness. I have just about eliminated [sic] the pains and the numbness is gone.”
• “[M]y results with Cardio Renew were pretty amazing! My total cholesterol on 10-7-05 was 291 …. LDL [bad cholesterol] was 197! … I took it [Cardio Renew] for 4 weeks …. I went back for another blood test on 2-16-06. My total cholesterol was 225!!! My bad cholesterol was down to 1431”
• “I was in constant pain, left arm and shortness of breath. I’ve just finished my forth [sic] week [taking Cardio Renew]. The pain in my left arm is gone….”
• “I have been taking Cardio Renew less than two weeks ‘” ! No angina, … and have cut the prescription BP [Blood Pressure] medication out. Reduced the diabetes medication to half.”
• “I had such tremendous results in just a few days [of taking Cardio Renew] for my arthritis ….”

Furthermore, videos posted on your websites

include testimonials and other claims that establish the intended use of Cardio Renew as a drug.

Examples of claims found on the videos include, but are not limited to:

“News Report: Oral EDTA Chelation”:
• “This is the alternative to drugs…. EDTA could be the key to unlocking the mystery of heart disease.”
• “My health is so many times better than before Cardio Renew. I have no symptoms of plaque buildup….”

“Today’s Health: Chelation Therapy”:

• “If blockage is found … some patients are trying an alternative therapy called EDTA chelation…. It is also believed by many that this process helps to reduce clogging in the arteries.”
• “With chelation therapy, we find that patients who have angina pectoris … improve — the pain disappears, they’re able to walk further”

The claims quoted above are supplemented by the metatags used to bring consumers to your website, www.cardiorenew.com. through Internet searches. These metatags include: “parkinsons disease … heart disease … fibromyalgia, hypertension, cardiovascular disease.”

Cardiorestore:
On your home page:

• “L-Arginine [an ingredient in your product] can also help reduce the risk of vascular and heart disease, high blood pressure, strokes and high cholesterol levels.”
• “N-Acetyl-Cysteine [an ingredient in your product] … [can] help prevent influenza infection.”

Your webpage titled “Chelation Therapy Health Conditions” states, “Below are conditions that Chelation Therapy has helped improve” followed by a list including the following:

• “Alzheimer’s disease Angina … Arteriosclerosis … Autoimmune disease … Bursitis … Cardiac Arrhythmia Cardiovascular Disease (CVD) … Coronary Artery Disease … Diabetes Mellitus … Diabetic Neuropathy … Diabetic Retinopathy … Erectile Dysfunction (ED) / Impotence … Fibromyalgia … Gangrene … Glaucoma … Heart Failure … Heavy Metal Poisoning … Hypertension/High Blood Pressure Multiple Sclerosis Osteoarthritis Parkinson’s disease … Raynaud’s Disease Rheumatoid Arthritis Scleroderma Stroke prevention.”

In addition, your website www.cardiorestore.com contains disease claims in the form of personal testimonials. The following are excerpts from a webpage entitled “Customer Testimonials:”

• “My son … is now using it [Cardio Restore] and in two weeks his blood pressure has gone down to normal..”
• “I was told by my doctor that 1 had over 80% blockage in my left Carotid Artery and 60% in my right …. I ordered your Chelation Plus Program [a package that includes Cardio Restore] and began the process…. I completed the program and then got checked out again and the blockage in both of my Carotid Arteries had decreased each by 35%.”
• “I started taking Cardio Restore about a month ago for my Angina. Not only is the angina gone….”

On your web page titled “Common Questions and Answers:”

• “Cardio Restore’s EDTA helps keep the stent from accumulating plaque and removes mineral build up that has formed around it, this keeps it clean…. [A] lot of our clients have avoided stent implantation. EDTA chelation removes the unwanted minerals and metals causing blood to flow easier, reducing the need for a stent.”
• “Does chelation treatment benefit arthritis?
Yes, EDTA … helps reduce inflammation in the joints…. Chelation therapy may be helpful for rheumatoid arthritis patients….”
• “Does chelation treatment benefit diabetes?
Yes, EDTA has shown to be effective in preventing complications of diabetes…. It has been reported that patients who have received chelation therapy have less amputations, less blindness, less renal dialysis, and other diabetes complications, than those on conventional treatments.”

The claims quoted above are supplemented by metatags used to bring consumers to your website www.cardiorestore.com through Internet searches. These metatags include: “unblocked arteries, unclogging arteries, artery blockage, artery plaque….”

Oralchelationblog:

In addition, your website www.oralchelationblog.comincludes many of the claims found on your other websites and cited above as well as direct links to www.cardiorenew.com. Examples of claims include the following:

• “If you are currently living with heart disease, high blood pressure, senile dementia, or macular degeneration, look into chelation therapy…. For a full list of diseases and illnesses that benefit from EDTA, click here [hyperiink to the “Benefits of Chelation Therapy” list of diseases found on www.cardiorenew.com)…

Your products are not generally recognized as safe and effective for the above referenced uses and therefore, the products are “new drugs” under section 201(p) of the Act [21 U.S.C. § 321(p)). New drugs may not be legally marketed in the U.S. without prior approval from FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)). FDA approves a new drug on the basis of scientific data submitted by a drug sponsor to demonstrate that the drug is safe and effective.

Furthermore, because your products “Cardio Renew” and “Cardio Restore” are offered for conditions that are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners, adequate directions cannot be written so that a layman can use the products safely for their intended uses. Thus, their labeling fails to bear adequate directions for their intended uses, causing them to be misbranded under section 502(f)(1) of the Act [21 U.S.C. § 352(f)(1)). The introduction of a misbranded drug into interstate commerce is a violation of § 301 (a) of the Act [21 U.S.C. § 331(a)).

The above violations are not meant to be an all-inclusive list of deficiencies in your products and their labeling. The unlawful disease treatment and prevention claims on your website are too numerous to list in this letter. It is your responsibility to ensure that products marketed by your firm comply with the Act and its implementing regulations. We advise you to review your website, product labels, and other labeling and promotional materials for your products to ensure that the claims you make for your products do not cause them to violate the Act.

You should take prompt action to correct the violations described above and prevent their future recurrence. Failure to do so may result in enforcement action without further notice. Sections 302 and 304 of the Act [21 U.S.C. §§ 332 and 334] authorize the seizure of illegal products and injunctions against manufacturers and distributors of those products.

Please notify this office, in writing, within 15 working days of the receipt of this letter, of the specific steps you have taken to correct the violations noted above and to assure that similar violations do not occur. Include any documentation necessary to show that correction has been achieved. If corrective actions cannot be completed within 15 working days, state the reason for the delay and the time within which the corrections will be completed.

Your response should be directed to, Tyra S. Wisecup, Compliance Officer, U.S. Food and Drug Administration. If you have any questions regarding any issues in this letter, please contact Ms. Wisecup at the address on the letterhead or (612) 758-7114.

Sincerely,

/s/

Gerald  J. Berg
Director
Minneapolis District

 

FDA Warning Letter – Dr. Rhonda Henry

October 12, 2010
WARNING LETTER
Via UPS

Dr. Rhonda Henry
247 La Costa Ave.
Dayton, NV 89403

Dear Dr. Rhonda Henry:

This is to advise you that the Food and Drug Administration (FDA) has reviewed your website at the internet address www.drhenry.com in July 2010 and has determined that the products, “Pure Heart,” “Melatonin,” “Flaxseed Meal,” “DHEA” and “Cardio Chelate (H-870)” are promoted for conditions that cause the products to be drugs under section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(g)(1)(B)].

The therapeutic claims on your website establish that the products are drugs because they are intended for use in the cure, mitigation, treatment, or prevention of disease.  The marketing of the products with these claims violates the Act.

Examples of some of the claims observed on your website include:

On a webpage at the Dr. Rhonda’s Health Store entitled, “Lose Weight Permanently By Eating”:

Pure Heart

• “[T]here is a completely safe … therapy that can prevent and even reverse heart disease”
•  “The results showed a superior clinical improvement in the Pure Heart group including:

o Decrease of LDL cholesterol
o Increase of HDL cholesterol
o Moderate to Dramatic decrease in angina
o Increase in total blood flow through previously occluded vessels
o Improvement in feeling of depression
o Recovery of myocardial function in previous ischemic and necrotic areas
o Reduction in tachycardia upon stress exercise”

• “The ingredients in Pure Heart appear to be capable of partially or completely reducing ischemia.”

•  “Pure Heart was created to help prevent the changes in the blood vessels which result in heart disease.”

Melatonin

• “Melatonin boosts the immune system reducing the likelihood and severity of infectious diseases, it is a super antioxidant that protects cells from free radical damage, slows the growth of tumors, regulates blood pressure, wards off heart disease, prevents cancer….helps control Parkinson’s Disease, stops or delays the formation of cataracts….”

Flaxseed Meal

• “The dynamic health benefits [of Flaxseed Meal] include: lowered blood pressure … and anti-cancer benefits.”

DHEA

• “Research has found DHEA to have significant anti-obesity … anti-cancer effects.”
• [L]ow DHEA levels correlate to increased risk of cancer, heart disease, osteoporosis, obesity, diabetes …”
• “Scientific research has linked increased levels of DHEA with reduced risk of most degenerative diseases ….”

Cardio Chelate (H-870)

• “Oral Chelation Formula Removes Plaque that Clogs and Hardens Arteries.”
• “Ayurvedic Herbs Work on the Cause of Heart Disease.”
• “This balanced herbal formula displays the following properties:

o “Pushkarmul and kut have beta blocking like activity.”
o “Arjuna has antihypertensive calcium channel blocker activity.”
o “Gugul has hypolipidemic and antithrombic properties.”
o “Shankhpushpi, arjuna and jalneem are … antihypertensive.”
o “Kut has antidiabetic properties.”
o “Gugul decreases obesity … ”

• “[B]romelain, an enzyme from pineapple, and Papain … cleanse the arteries.”
• “These enzymes break down fibrin, inhibit clotting and promote normal healing of surface lesions.”

Your website also contains disease claims in the form of personal testimonials. The following are excerpted from a webpage entitled “Dr. Rhonda Henry’s Health Test”:

•  “Recently, an excruciatingly painful arthritis flare up in my knees …. Dr. Rhonda heard of my pain, she came in like an angel, bearing a bag of supplements ….  Within 24 hours, my condition turned around.  The inflammation left, the mobility increased.”
• “8 years ago, I was a very sick person.  I had battled colitis, diverticulitis, Epstein-Barr virus and low blood sugar.  I spent thousands of dollars on tests and doctor bills trying to find an end to all my health problems.  I picked up parasites in the Yucatan Peninsula …. I was down 93 pounds, couldn’t digest food, and was weak
• and dizzy all the time … I now eat and digest my food, lift weights 3 times a week, and have energy to spare.”

The claims quoted above are supplemented by the metatags used to bring consumers   to your website through Internet searches.  The metatags include “diabetes”, “arthritis”, “depression”, “menopause”, “peri-menopause”, “Candida”, “digestive disorders”, “osteoporosis”, and “infections”.

Your products are not generally recognized as safe and effective for the above referenced uses and therefore, the products are “new drugs” under section 201(p) of the Act [21 U.S.C. § 321(p)].  New drugs may not be legally marketed in the U.S. without prior approval from FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)].  FDA approves a new drug on the basis of scientific data submitted by a drug sponsor to demonstrate that the drug is safe and effective.

The above violations are not meant to be an inclusive list of deficiencies in your products and their labeling.  It is your responsibility to ensure that products marketed by your firm comply with the Act and its implementing regulations.  We advise you to review your website, product labels, and other labeling and promotional materials for your products to ensure that the claims you make for your products do not cause them to violate the Act.

You should take prompt action to correct the violations described above and prevent their future recurrence.  Failure to do so may result in enforcement action without further notice. The Act authorizes the seizure of illegal products and injunctions against manufacturers and distributors of those products [21 U.S.C. §§ 332 and 334].

Please notify this office, in writing, within fifteen (15) working days of the receipt of this letter, as to the specific steps you have taken to correct the violations noted above and to assure that similar violations do not occur.  Include any documentation necessary to show that correction has been achieved.  If corrective actions cannot be completed within fifteen working days, state the reason for the delay and the time within which the corrections will be completed.

Your response should be directed to Juliane K. Jung-Lau, Compliance Officer, U.S. Food and Drug Administration, 1431 Harbor Bay Parkway, Alameda, CA 94502.  If you have any questions regarding any issues in this letter, please contact Ms. Jung-Lau at 510-337-6793.

Sincerely,

/S/

Barbara J. Cassens
Director
San Francisco District

FDA Warning – Evenbetternow

October 12, 2010

WARNING LETTER
VIA UPS NEXT DAY

W/L 03-11

Mr. Donald Nichols
Ms. Andrea Nichols
Evenbetternow, LLC
447 W. Silvertip Road
Oro Valley, AZ 85737
Evenbetternow, LLC
1870 W. Prince Road, Suite 54
Tucson, AZ 85705
Re: Kids Chelat Heavy Metal Chelator, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, Natur-Leaf, Kids Clear Detoxifying Clay Baths, EBN Detoxifying Bentonite Clay, and Heavy Metal Screen Test
Dear Mr. and Ms. Nichols:
This letter concerns your firm’s marketing of several products, including but not limited to, Kids Chelat Heavy Metal Chelator, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, Natur-Leaf, Kids Clear Detoxifying Clay Baths, EBN Detoxifying Bentonite Clay, and Heavy Metal Screen Test on your websites:
These (and other) products are marketed in violation of provisions of the Federal Food, Drug, and Cosmetic Act (the Act) as described below.
According to the products’ labeling, Kids Chelat Heavy Metal Chelator, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, and Natur-Leaf are intended to cure, mitigate, treat, or prevent disease conditions. Statements documenting these intended uses include, but are not limited to, the following:

Kids Chelat Heavy Metal Chelator

• “Guaranteed to remove heavy metal ions from the body . . . Kids-ChelatTM contains EDTA, an amino acid that is so effective at removing unwanted minerals and metals from
the body, that is has been the standard FDA approved treatment for lead, mercury, aluminum and cadmium poisoning for more than 50 years.”
• “I recently ordered the Kids Chelat™ and Kids Clear clay baths for my 10 year old son. The results were astounding. My son was able to transition out of his special education classroom at school and he needs his classroom assistant much less.”
• “The Kids Chelat™ totally changed my autistic son from a hand flapping hyper kid to a sweet mellow angel.”
Bio-Chelat Heavy Metal Chelator

• “As a preventative measure, Bio-Chelat™ keeps any unbound heavy metals ions from being absorbed (or re-absorbed) by the body . . . whether it be metal ions from food, amalgams, or the environment. Bio-Chelat™ has its greatest value for sub-acute or chronic heavy metal toxicity.”
• “My son Anthony is 5 years old and has behavioral and developmental challenges . . . Within a couple of weeks of using Bio-Chelat™ on Anthony. . . his speech returned at a higher level than his usual immature echolaic-type dialogue.”
• “[D]iagnosed as autistic . . . . He started taking Bio-Chelat™ . . . . He became quieter, and his speech improved . . . . Also, he demonstrated improved social response.”
• “I take Bio-Chelat and it has really helped with my neuropathy which creates a burning, stabbing pain throughout my body.”
• “I suffered from heavy pollen allergies . . . However, soon after I started with the product I was almost completely free of any symptoms.”
Behavior Balance DMG Liquid

• “My grandson is reading outloud from books. After being on the spectrum for 3 years and had lost his speech at 3 yrs. we are delighted at his progress! Behavior Balance- DMG™ contributed to this important development.”
AlkaLife Alkaline Drops

• “Flush Out Harmful Acid Waste & Reverse Aging, Illness and Disease!”
• “I have suffered with acid reflux for the past 6 years, and have taken prescription medication (proton pump inhibitors) . . . . Since using the alkalizing drops . . . I have been finally able to get off all the medicines.”
• “I was diagnosed with IC [interstitial cystitis] . . . . I purchased your product, AlkaLife drops . . . . [T]his product . . . will lead me to better pain management, if not a cure.”
NutriBiotic Grapefruit Seed Extract

• “A powerful anti-bacterial and anti-fungal agent.”
Natur-Leaf
• “We have seen patients who have irritable bowel syndrome, spastic colons, abdominal cramping, rheumatoid arthritis, cystis [sic], fibromyalgia, hay fever, asthma, allergies to foods and medications, benign prostate hypertrophy and acne, have their symptoms completely reverse and the patients return to normal health.”
In addition to the above-listed products that you market as supplements, your firm also markets Kids Clear Detoxifying Clay Baths and EBN Detoxifying Bentonite Clay. According to product labeling, Kids Clear Detoxifying Clay Baths and EBN Detoxifying Bentonite Clay are intended to cure, mitigate, treat, or prevent disease conditions or to affect the structure or function of the body. Statements documenting these intended uses include, but are not limited to, the following:
Kids Clear Detoxifying Clay Baths

• “We highly recommend this product to any parent looking for a new and different way to combat Autism and the toxins that attribute to this disorder.”
• “Kids Clear™ Detoxifying Clay Baths not only draw out chemical toxins and pollutants from the body, they also assist in pulling out heavy metals that many doctors agree are a causative factor in the development of neurological and behavioral symptoms.”
• “After using clay baths, a number of parents of an autistic child have noticed dramatic improvement.”
• “What a change! Our almost 5 year old son who is on the spectrum is now doing great. After just the first bath, my husband and I saw results! He’ll turn to look at us (in the eyes) after calling his name only once! He’s using the right words to communicate, and in sentences!! And best of all, he’s smiling and laughing, and just seems happier!”
EBN® Detoxifying Bentonite Clay

• “EBN® Clay Baths assist in the removal of both metal and chemical toxins, such as food additives, preservatives, radiation toxins, formaldehyde, cigarette toxins, pesticides, and so on.”
• “In addition to being an excellent internal detoxifying agent, our clay can be very helpful for acute upset stomach, indigestion and diarrhea.”
• “Our clay was used in Malawi . . . to inhibit the incidence of diarrhea in infants and children.”
• “For many years I suffered from migraines . . . and after about 3 months there was a huge improvement.”
• Toxins play a major role in ALS [Amyotrophic Lateral Sclerosis] and other neurological disorders, so neutralizing these toxins is highly important. Two very easy, inexpensive and effective ways to do this is with EBN® Detoxifying Clay Baths and Bio-Chelat™ Heavy Metal Chelator.
Kids Chelat Liquid Chelation Drops, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, and Natur-Leaf are represented as dietary
supplements.
However, these products are drugs, as defined by section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (“the Act”), 21 U.S.C. § 321(g)(1)(B), because they are intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease. Kids Clear Detoxifying Clay Baths and EBN Detoxifying Bentonite Clay are also drugs under section 201(g)(1) of the Act, 21 U.S.C. § 321(g)(1), because they are intended to affect the structure or function of the body and/or intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man. We note that certain versions of Kids Clear Detoxifying Clay Baths and EBN Detoxifying Bentonite Clay represents these products as dietary supplements. To the extent that these products are not intended for ingestion, they are not dietary supplements as defined by section 201(ff) of the Act, 21 U.S.C. § 321(ff).
Moreover, Kids Chelat Heavy Metal Chelator, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, Natur-Leaf, Kids Clear Detoxifying Clay Baths, and EBN Detoxifying Bentonite Clay are “new drugs” as defined by section 201(p) of the Act, 21 U.S.C. § 321(p), because they are not generally recognized as safe and effective for use and under the conditions prescribed, recommended, or suggested in its labeling. Under sections 301(d) and 505(a) of the Act, 21 U.S.C. §§ 331(d) and 355(a), new drugs may not be introduced or delivered for introduction into interstate commerce unless an FDA-approved application is in effect for them. FDA-approved applications are not in effect for these products. Thus, the sale of the above-listed products violates these provisions of the Act.
Furthermore, Kids Chelat Heavy Metal Chelator, Bio-Chelat Heavy Metal Chelator, Behavior Balance DMG Liquid, AlkaLife Alkaline Drops, NutriBiotic Grapefruit Seed Extract, Natur-Leaf, Kids Clear Detoxifying Clay Baths, EBN Detoxifying Bentonite Clay are offered for conditions, such as (but not limited to) autism, heavy metal poisoning, and interstitial cystitis, which are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners. Therefore, adequate directions cannot be written so that a layman can use them safely for their intended uses. Thus, your products’ labeling fails to bear adequate directions for their intended uses, causing them to be misbranded under section 502(f)(1) of the Act, 21 U.S.C. § 352(f)(1). These products are not exempt under 21 C.F.R. §§ 201.100(c)(2) and 201.115 from the requirement that labeling bear adequate directions for use because these products lack approved applications. Section 301(a) of the Act, 21 U.S.C. § 331(a), prohibits the introduction of a misbranded drugs into interstate commerce. Accordingly, the sale of the above-listed products violates these provisions of the Act.
In addition to the new drugs that you market and sell on your websites in violation of the Act, you also market and sell the Heavy Metal Screen Test in violation of the Act.  The Heavy Metal Screening Test is a device because it is intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals. Your websites
state the following regarding the Heavy Metal Screen Test:
• “By taking a urine sample and mixing it with the test solutions . . . it determines immediately the presence of unbound heavy metal ions in your urine.”
• “The Heavy Metal Screen Test is a wonderful way to know if you have heavy metals in your body AND to show you the progress along the way as you use the Bio-Chelat and EBN Detox clay baths.”
• “The Heavy Metal Screen Test gives you a quick, reliable method for determining if electrically active heavy metal ions are present (ie. being excreted through the urine) at a high, medium, or low concentration, or not at all.”
• “This test is most useful in determining if your body’s detoxification pathways are compromised or not.”
The Heavy Metal Screen Test, used to detect heavy metals in human urine, is adulterated under section 501(f)(1)(B) of the Act, 21 U.S.C. §351(f)(1)(B), because an approved application for premarket approval (PMA) pursuant to section 515(a) of the Act, § 21 U.S.C. 360e(a) or an approved application for an investigational device exemption (IDE) under section 520(g) of the Act, 21 U.S.C. §360j(g), are not in effect for it. The Heavy Metal Screen Test is also misbranded under section 502(o) of the Act, 21 U.S.C. §352(o), in that it was manufactured, prepared, propagated, compounded or processed in an establishment not duly registered under section 510 of the Act, 21 U.S.C. §360; not included in a list required by 510(j), 21 U.S.C. §360(j); and notification or other information respecting the device was not provided to the FDA as required by section 510(k) of the Act, 21 U.S.C. §360(k). The issues and violations cited in this letter are not an all-inclusive statement of violations that exist in connection with your products and websites. You are responsible for investigating and determining the causes of the violations identified above and for preventing their recurrence or the occurrence of other violations. It is your responsibility to ensure that your firm complies with all requirements of federal law and FDA regulations.
You should take prompt action to correct the violations cited in this letter and any other violations you may have. Failure to promptly correct such violations may result in legal action, without further notice, including, without limitation, seizure and injunction. Other federal agencies may take this Warning Letter into account when considering the award of contracts.
Within fifteen working days of receipt of this letter, please notify this office in writing of the specific steps that you have taken to correct violations. Include an explanation of each step being taken to prevent the recurrence of violations, as well as copies of related documentation. If you cannot complete corrective action within fifteen working days, state the reason for the delay and the time within which you will complete the correction. Additionally, if another firm manufactures the products identified above, your reply should include the name and address of the manufacturer. If the firm from which you receive the products is not the manufacturer, please include the name of your supplier in addition to the manufacturer. Your response should be sent to:
Mr. Blake Bevill
Director, Compliance Branch
Food and Drug Administration
Los Angeles District Office
19701 Fairchild
Irvine, CA   92612
If you have any questions about the content of this letter, please contact Dr. William Vitale, Compliance Officer, at 949-608-2919.
A description of the new drug approval process can be found on FDA’s internet website athttp://www.fda.gov/Drugs/DevelopmentApprovalProcess/default.htm.
In addition, information regarding approval or clearance for devices is described at
Any questions you may have regarding this process should be directed to the Food and Drug Administration, Division of Drug Information, Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, WO51-2201, Silver Spring, Maryland 20993.
Sincerely yours,
/S/
Alonza E. Cruse

District Director

Hormonal Health

October 12, 2010
W/L 04-11

Mr. Richard D. Brooks
Ms. Joan R. Campbell
Hormonal Health, LLC
357 West 2nd Street Suite 1A
San Bernardino, California  92401

Mr. Richard D. Brooks
Ms. Joan R. Campbell
Hormonal Health, LLC
1213 Goldfield Avenue
Carson City, Nevada  89701

Dear Mr. Brooks and Ms. Campbell:

This letter concerns your firm’s marketing of its Kelatox suppository product and its METALDETECTOR Instant Toxic Metals Test, on your websites:

This product is marketed in violation of provisions of the Federal Food, Drug, and Cosmetic Act (the Act) as described below.

According the labeling, Kelatox is intended to affect the structure or function of the body of man or other animals and/or intended to cure, mitigate, treat, or prevent disease conditions.  Statements documenting these intended uses include, but are not limited to, the following:

• “Kelatox . . . removes a wide range of toxic metals including Mercury, Lead and Aluminum from the body.”

• “Kelatox® uses Calcium Disodium EDTA . . . recommended . . . for lead poisoning and other toxic heavy metal conditions . . . as far ranging as decreased circulation, degenerative diseases such as Alzheimer’s, diabetes, decreased adrenal gland function and Autism. ”

• “The primary cause of endothelial dysfunction is the build up of heavy metals in this [endothelial] lining . . . .  The EDTA in Kelatox will remove heavy metals from the endothelium helping it to produce nitric oxide thereby allowing the blood vessels to relax increasing the blood flow.”

• “We have seen changes in patients with chronic fatigue, fibromyalgia, neurological diseases, depression, skin problems, headaches, and many more conditions.  This product is beneficial to help your patients heal.”

• “My husband was diagnosed with Parkinson’s Disease recently. . . .  Kelatox was ordered and started.  Within weeks, he was feeling better.  In eight weeks his massage therapist noticed a difference in his overall body . . . She was giving him massages for years and was never able to work “deep in his muscles” until he took Kelatox.”

• “I . . . have been taking IV EDTA since 1998 for macular degeneration.  I’ve recently switched to EDTA chelation suppositories. . . .  Because they are working so well, I am planning on dropping IV EDTA and solely using the chelation suppositories.”

• “I suffer from Peripheral Neuropathy and had lost all feeling in my legs. . . .  One month after I started Kelatox, I regained the sense of feeling completely in my right leg and partially in the left.”

Your firm markets Kelatox as a dietary supplement.  Because this product is a suppository and not intended for ingestion, it is not a dietary supplement as defined by section 201(ff) of the Act, 21 U.S.C. § 321(ff).  Rather, this product is a drug, as defined by section 201(g)(1) of the Act, 21 U.S.C. § 321(g)(1), because it is intended to affect the structure or function of the body and/or intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man.

Moreover, Kelatox is a “new drug” as defined by section 201(p) of the Act, 21 U.S.C. § 321(p), because it is not generally recognized as safe and effective for use under the conditions prescribed, recommended, or suggested in their labeling.  Under sections 301(d) and 505(a) of the Act, 21 U.S.C. §§ 331(d) and 355(a), a new drug may not be introduced or delivered for introduction into interstate commerce unless an FDA-approved application is in effect for it.  Your sale of Kelatox suppositories without an approved application violates these provisions of the Act.

Furthermore, Kelatox is offered for conditions such as, but not limited to, lead poisoning, Alzheimer’s disease, autism, endothelial dysfunction, Parkinson’s disease, macular degeneration, and peripheral neuropathy, which are not amendable to self-diagnoses and treatment by individuals who are not medical practitioners.  Therefore, adequate directions cannot be written so that a layman can use Kelatox safely for its intended uses.  Thus, the labeling of Kelatox suppositories fails to bear adequate directions for its intended uses, causing it to be misbranded under section 502(f)(1) of the Act, 21 U.S.C. § 352(f)(1).  Kelatox is not exempt, under 21 C.F.R. §§ 201.100(c)(2) and 201.115, from the requirement that its labeling bear adequate directions for use because Kelatox lacks an approved application.  The introduction or delivery for introduction into interstate commerce of this misbranded drug violates section 301(a) of the Act, 21 U.S.C. §331(a).

In addition to the new drug that you market and sell on your websites in violation of the Act, you also market and sell the METALDETECTOR Instant Toxic Metals Test in violation of the Act.  The METALDETECTOR Instant Toxic Metals Test is a device because it is intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals.  Your website www.kelatox.com states the following regarding the METALDETECTOR Instant Toxic Metals Test:

• “Test for the presence of toxic metals in urine or water, with this quick and convenient in-home test.”

• “The METALDECTOR™ Instant Toxic Metals Test readily detects free, electrically-active heavy metal ions.”

• “For anyone who is serious about avoiding degenerative diseases facing the human race, getting tested for heavy metals is more important than ever before.”

The METALDETECTOR Instant Toxic Metals Test, used to detect heavy metals in human urine, is adulterated under section 501(f)(1)(B) of the Act, 21 U.S.C. §351(f)(1)(B), because an approved application for premarket approval (PMA) pursuant to section 515(a) of the Act, 21 U.S.C. §360e(a) or an approved application for an investigational device exemption (IDE) under section 520(g) of the Act, 21 U.S.C. §360j(g), are not in effect for it.  The METALDETECTOR Instant Toxic Metals Test is also misbranded under section 502(o) of the Act, 21 U.S.C. §352(o), in that it was manufactured, prepared, propagated, compounded or processed in an establishment not duly registered under section 510 of the Act, 21 U.S.C. §360; not included in a list required by 510(j), 21 U.S.C. §360(j); and notification or other information respecting the device was not provided to the FDA as required by section 510(k) of the Act, 21 U.S.C. §360(k).

The issues and violations cited in this letter are not intended to be an all-inclusive statement of violations that exist in connection with your product.  You are responsible for investigating and determining the causes of the violations identified above and for preventing their recurrence or the occurrence of other violations.  It is your responsibility to ensure that your firm complies with all requirements of federal law and FDA regulations.

You should take prompt action to correct the violations cited in this letter.  Failure to promptly correct these violations may result in legal action, without further notice, including, without limitation, seizure and injunction.  Other federal agencies may take this Warning Letter into account when considering the award of contracts.

Within fifteen working days of receipt of this letter, please notify this office in writing of the specific steps that you have taken to correct violations.  Include an explanation of each step being taken to prevent the recurrence of violations, as well as copies of related documentation.  If you cannot complete corrective action within fifteen working days, state the reason for the delay and the time within which you will complete the correction.  Furthermore, please advise this office what actions you will take to address product that you have already distributed.  Additionally, if another firm manufactures the product identified above, your reply should include the name and address of the manufacturer.  If the firm from which you receive the product is not the manufacturer, please include the name of your supplier in addition to the manufacturer.

Your response should be sent to:

Blake Bevill
Director, Compliance Branch
Food and Drug Administration
19701 Fairchld
Irvine, CA  92612-2506

If you have any questions regarding any issues in this letter, please contact Marco Esteves, Compliance Officer at (949) 608-4439

A description of the new drug approval process can be found on FDA’s internet website athttp://www.fda.gov/Drugs/DevelopmentApprovalProcess/default.htm.  In addition, information regarding approval or clearance for devices is described athttp://www.fda.gov/cdrh/devadvice/3122.html.  Any questions you may have regarding this process should be directed to the Food and Drug Administration, Division of Drug Information, Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, WO51-2201, Silver Spring, Maryland  20993.

Sincerely,

/S/
Alonza E. Cruse
District Director

cc: Jay Salmon
World Health Products, LLC
12685 South 125 East
Draper, Utah  84020

Marv Bateman
1189 E. Pinion St.
Washington, Utah  84780

Zayin of Utah Corporation
1022 W Smithsonian
Apple Valley, Utah  84737

FDA Warning – Artery Health Institute

October 12, 2010
WARNING LETTER NYK-2011-02

VIA UPS

Howard Sousa
The Artery Health Institute, LLC
45 East 89th Street
New York, NY 10128

Dear Mr. Sousa:

This is to advise you that the Food and Drug Administration (FDA) reviewed your website atwww.arteryhealthinstitute.com in June 2010 and has determined that your product “Advanced Formula EDTA Oral Chelation” is promoted for conditions that cause the product to be a drug under section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(g)(1)]. The claims on your website establish that the product is a drug because it is intended for use in the cure, mitigation, treatment, or prevention of disease. The marketing of your product with these claims violates the Act.

Examples of some of the claims observed on your website include:

• “UNCLOG arteries and restore cardiovascular function”
• “This completely safe and natural therapy has been used successfully for over 50 years … Plaque is dissolved throughout your entire circulatory system. It can reverse atherosclerosis, lower cholesterol levels and blood pressure and help to prevent heart attacks and strokes!”
• “[P]atients … suffering from angina and coronary artery disease, symptoms dropped dramatically.”
• “Chelation therapy appeared to be a powerful antidote to- and preventative against-atherosclerosis, arthritis, kidney stones and otosclerosis ….”
• “EDTA chelation is one of the most effective, least expensive, and safest treatments for heart disease ever developed”
• “EDTA … REDUCES CHOLESTEROL”
• “By improving calcium and cholesterol metabolism EDTA can help to lower cholesterol, the principal component of atherosclerotic plaque.”
• “Garlic [an ingredient in Advanced Formula EDTA Oral Chelation] is believed to work by making blood less “sticky,” preventing the clinging of plaque to arterial walls…. [G]arlic may have more than a preventive effect and even possibly … ‘a curative role in arteriosclerosis therapy (plaque regression)’.”
• “Some dangerous heavy metals that are removed from your body using EDTA chelation therapy are:
o MERCURY: Some symptoms: … hyperactivity, migraines …
o LEAD: Some Symptoms: ADD, cardiovascular disease, impotence, liver
dysfunction
o CADMIUM: Some Symptoms: Arthritis, cancer, lung disease, kidney disease,
vascular disease, high cholesterol, cardiovascular disease
o ARSENIC: Some Symptoms: Liver dysfunction … chronic anemia
o ALUMINUM: Some Symptoms: liver dysfunction, neuromuscular disorders”
• “[C]onsistently observed a reduction of serum cholesterol by an average 20% or more in … patients who use oral chelation.”
Your website also contains disease claims in the form of personal testimonials from Dr. Garry Gordon, including:
• “I had a patient … who could never get her cholesterol below 500. Once she started taking 6 tablespoons a day of the EDTA-based chelation formula, she got down to 200. So this stuff can work wonders.”
• “The more chelation we give people, the less osteoporosis they have ….”

The disease claims quoted above are supplemented by the metatags used to bring consumers to your website through Internet searches. The metatags include: “cardiovascular disease” and “clogged arteries.”

Your product is not generally recognized as safe and effective for the above referenced uses and, therefore, the product is a “new drug” under section 201(P) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally marketed in the U.S. without prior approval from FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)]. FDA approves a new drug on the basis of scientific data submitted by a drug sponsor to demonstrate that the drug is safe and effective.
Furthermore, your product is offered for conditions that are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners; therefore, adequate directions for use cannot be written so that a layperson can use these drugs safely for their intended purposes. Thus, your product is misbranded within the meaning of section 502(f)(1) of the Act [21 U.S.C. § 352(f)(1)], in that the labeling fails to bear adequate directions for use. The introduction of a misbranded drug into interstate commerce is a violation of section 301(a) of the Act [21 U.S.C. § 331(a)].
The above violations are not meant to be an all-inclusive list of deficiencies in your products and their labeling. It is your responsibility to ensure that all of your products and labeling are in compliance with the laws and regulations enforced by FDA. You should take prompt action to correct the violations. Failure to promptly correct these violations may result in regulatory action without further notice, such as seizure and/or injunction.
Please notify this office in writing within fifteen (15) working days from your receipt of this letter as to the specific steps you have taken to correct the violations noted above and to assure that similar violations do not occur. Your response should include any documentation necessary to show that correction has been achieved. If you cannot complete all corrections before you respond, please explain the reason for the delay and state the date by which the corrections will be completed.
Please send your reply to the attention of Lillian C. Aveta, Compliance Officer, New York District Office, Compliance Branch, Food and Drug Administration, 158-15 Liberty Ave., Jamaica, NY 11433. If you have any questions regarding any issue in this letter, please contact Ms. Aveta at 718-662-5576.
Sincerely,

/S/
Ronald M. Pace
District Director

FDA Warning – Maxam Nutraceutics

October 12, 2010
VIA UPS

In reply refer to Warning Letter SEA 11-01
WARNING LETTER

James G. Cole, CEO
Maxam Nutraceutics/Maxam Laboratories
1020-D Wasco Street
Hood River, Oregon 97031

Re: PCA-Rx, PC3x, AFX, AD-Rx, AN-Rx, Anavone, AV-Rx, BioGuard, BSAID, CF-Rx, CreOcell, Dermatotropin, Endotropin, GTF-Rx, IM-Rx, Keto-Plex, Natural Passion, NG-Rx, NX-Rx, OR-Rx, Oxy-Charge, PN-Rx, Ultra-AV, Ultra Pure Yohimbe, and the Heavy Metal Screening Test

Dear Mr. Cole:

This letter concerns your firm’s marketing of your products: PCA-Rx, PC3x, AFX, AD-Rx, AN-Rx, Anavone, AV-Rx, BioGuard, BSAID, CF-Rx, CreOcell, Dermatotropin, Endotropin, GTF-Rx, IM-Rx, Keto-Plex, Natural Passion, NG-Rx, NX-Rx, OR-Rx, Oxy-Charge, PN-Rx, Ultra-AV, Ultra Pure Yohimbe, and the Heavy Metal Screening Test on your website, www.maxamlabs.com. These products are marketed in violation of provisions of the Federal Food, Drug, and Cosmetic Act (the Act) as described below.
According to labeling, your products are intended to affect the structure or function of the body of man or other animals and/or intended to cure, mitigate, treat, or prevent disease conditions.
Statements documenting these intended uses include, but are not limited to, the following:

PCA-Rx

• “Try our oral chelation therapy called clathration for autism, Alzheimers, allergies, heavy metal detox and more.”
• “Removes heavy metals, toxins, mycoplasmas and cardio and cerebral vascular plaque.”
• “Some older users of PCA-Rx have remarked a definite improvement in thought process and recall ability ….”

• “Strong Relief For Uterine Fibroids … After 3 months of using PCA-Rx from Maxam, the growths resolved completely.”

PC3x

• “I have been giving this to a friend of mine that has lung problems from chemical exposure and had to use an inhaler to breath [sic] when out in the heat. After just two months of use … he showed a 51% increase in lung capacity.”
• “Aids in and accelerates the cellular detoxification process.”
AFX (Autism Factor)
• “Restructures and repairs all pathways, including the brain, nervous system, thyroid, growth hormone and immune function.”
• “Maxam constantly fine-tuned AFX to enhance its efficacy, addressing all aspects of Autism Spectrum/ADD/ADHD/RS or any other neural developmental disorders ….”

AD-Rx

• “AD-Rx enhances serotonin (5-HT) function in the body.”
• “[N]atural treatment for mood disorders, anxiety, fatigue, insomnia, eating disorders, Post-Traumatic Stress Disorder (PTSD), Premenstrual Syndrome (PMS) and Obsessive-compulsive
disorder (OCD).”
AN-Rx (Pain Relief Anti-Anxiety Formula)

• “Relieves pain and anxiety, helps balance mood and has a calming effect.”
• “[H]elps with insomnia and interrupted sleep patterns.”

Anavone

• “Suppresses the catabolic hormone cortisol.”
• “[I]ncreases protein synthesis.”
• “Prevents muscle breakdown.”

AV·Rx


• “Diseases such as herpes, AIDS, the flu, mad cow disease and various types of cancer are all of viral or prion origin…. AV-Rx will help protect the body against diseases of viral or prion origin, as well assisting the body in the healing of these types of diseases.”
• “Herpes Relief – At Last!! … Within 24 hours of starting to take AV-Rx, Maxam Lab’s antiviral formula, her symptoms began to respond…. The client … even sprayed it externally on the vaginal membranes…. As a clinician, it is so wonderful to have clients get such an immediate response when the body has not been able to respond to any other treatment.”

BioGuard

• “Clean(s] and enhance(s] the immune system.”
• “Beneficial for intestinal bacteria and fungus, such as Candida yeast overgrowth.”

BSAID (Broad Spectrum Anti-Infective Disease)
• “Shown effective against latent residual viruses from old inoculations, measles, mumps, small pox, as well as HPV, EBV, CMV, HIV, etc.”
• “BSAID can also be used topically on areas of infection or injury.”
• “My son who is now 18 has had severe large clusters of cold sore breakouts since he was about 2 years old … I thought I would try BSAID for my son. IT WORKED WONDERS!!!He has not had a breakout in 2 years now.”
CF-Rx (Cellaflex Anti-Inflammatory Anti-Arthritic)
• “Anti-arthritic which stimulates regeneration and repair of all soft tissue, tendons, ligaments, muscle, skin (bruises). Cellaflex is also an anti-inflammatory which reduces pain in joint structures.”
• “[I]t is useful to nebulize the Cellaflex for lung diseases, especially asthma and other related pulmonary diseases.”
CreOcell (Creatinine Phosphokinase)
• “Enhances Endurance and Muscular Growth.”
• “Increased muscle nitrogen levels with lower protein intake, increased ATP level recovery and many of the positive benefits of a true anabolic compound without any of the negative side effects associated with toxic loading or anabolic steroid use.”
• “CreOcell is reported to give higher energy and endurance levels, harder more defined muscles, an increase in mental awareness and the most incredible “pump” users say they have ever experienced.”
Dermatropin
• “Dermatropin stimulates collagen, elastin regeneration, activates scar tissue repair, and reduces wrinkling and sun damage.”
Endotropin
• “Endotropin has been created to stimulate release of human growth hormone, stimulates full pituitary and hypothalamic function, luteinizing and follicle stimulating hormones, which, in turn, will stabilize estrogen and testosterone production.”

• “Endotropin will also stimulate adrenocorticotropic hormone (acth), which increases energy. Melanin, dopamine, serotonin, melatonin, and oxytocin are all stimulated as well…. Your entire endocrine system is covered. Endotropin may have just made growth hormone obsolete!”
GTF-Rx (Glucose Tolerance Factor)
• “GTF-Rx increases insulin sensitivity of cells, lowers insulin requirements, normalizes glucose levels, ameliorates symptoms of diabetes and accompanying chronic tissue degeneration.”
IM-Rx (Immune System Enhancement)
• “IM-Rx is an immune system modifier that down-regulates autoimmune dysfunction, to help alleviate symptoms of arthritis, lupus, multiple sclerosis and enhances T & B cell activity in response to infection.”

Keto-Plex

• “Increases Immunity/Assists in Weight Loss”
• “Keto-Plex … has measurable effects on increasing muscular density and hardness and promoting a defined, lean appearance. It also assists in weight loss and minimizes catabolism (break down) of muscle tissue.”
Natural Passion
• “Natural Passion Helps Increase:
o Libido
o Virility
o Sensitivity
o Desire for sexual intimacy”
NG-Rx (Neural Regeneration)
• “[D]esigned to … balance and correct the brain chemistry … and induce the formation and activation of neuro-pathways.”
• “NG-Rx … can help to reduce memory loss.”
• “It can stimulate your immune system.”
• “NG-Rx can also assist with weight loss, and can improve your mood when you are feeling a little down.”
• “I have had paralysis of the left side of my face for many years. I began using your NG-Rx on the advice of your friendly customer service staff. I am happy to report that after only ten days of being on your product, I am seeing changes in the amount of facial paralysis.”

NX-Rx (Neural Enhancer)

• “Stimulates nerve cell regeneration and repair in both the central and peripheral nervous system by encouraging the production of nerve growth factor.”
OR-Rx (Osteo Regeneration Hard Tissue Support)
• “This product assists your body with hard tissue repair of teeth and bones; up-regulates calcium and calcium absorption.”
• “Also beneficial for gum infections, soft teeth, broken bones, osteoporosis and osteoarthritis.”
• “OR-RX has the capability to pull bacterial infections from the oral cavity.”

Oxy-Charge

• “Oxy-Charge effectively increases muscle energy on a cellular level, oxygenates the hemoglobin in blood and eliminates carbon monoxide.”
PN-Rx (Pineal Stimulating Peptides)
• “PN-Rx stimulates pineal harmone production, up-regulates melatonin and sleep while down-regulating Prementrual Syndrome (PMS) and pain.”

Ultra-AV

• “A powerful growth hormone stimulant that effectively suppresses production of the hormone somatostatin (which inhibits growth-hormones) and has life extension and anti-aging properties.”
• “A ‘Fountain of Youth’ of sorts, that helps reverse biological aging, assists in regeneration of all tissues, is anabolic and aids in weight loss.”
Ultra Pure Yohimbe
• “Used in the treatment of male impotence.”
• “Promotes the stimulation of testosterone.”

Your firm markets the above-listed products as dietary supplements. However, your products are labeled as transmucosal sprays for sublingual administration. You also recommend that “It is also
beneficial to nebulize many of the Maxam products.”
In addition, your firm markets your products AV-Rx, BSAID, and CF-Rx for topical administration. Because these products are not intended for
ingestion, they are not dietary supplements as defined by section 201(ff) of the Act, 21 U.S.C. § 321(ff). Rather, these products are drugs, as defined by section 201(g)(1) of the Act, 21 U.S.C. §
321(g)(1), because they intended to affect the structure or function of the body and/or intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man.
Moreover, all of the above-listed products are “new drugs” as defined by section 201(P) of the Act, 21 U.S.C. § 321 (p), because they are not generally recognized as safe and effective for use under the conditions prescribed, recommended, or suggested in their labeling. Under sections 301(d) and 505(a) of the Act, 21 U.S.C. §§ 331(d) and 355(a), a new drug may not be introduced or delivered for introduction into interstate commerce unless an FDA-approved application is in effect for it. Your sale of your above-listed products, without an approved application, violates these provisions of the Act.

Furthermore, your above-listed products are offered for conditions which are not amendable to self-diagnoses and treatment by individuals who are not medical practitioners such as, but not limited to, autism, Alzheimer’s disease, heavy metal toxicity, uterine fibroids, mood disorders, impotence, asthma, diabetes, and infections including herpes, HIV (human immunodeficiency virus), and EBV (Epstein-Barr virus). Therefore, adequate directions cannot be written so that laymen can use your products safely for their intended uses. Thus, the labeling of your above-listed products fail to bear adequate directions for their intended uses, causing them to be misbranded under section 502(f)(1) of the Act, 21 U.S.C. § 352(f)(1). The above~listed products are not exempt, under 21 C.F.R. §§ 201.100(c)(2) and 201.115, from the requirement that their labeling bear adequate directions for use because they lack approved applications. The introduction or delivery for introduction into interstate commerce of these misbranded drugs violates section 301(a) of the Act, 21 U.S.C. § 331(a).
In addition to the new drugs that you market and sell on your website, www.maxamlabs.com in violation of the Act, you also market and sell the Heavy Metal Screening Test in violation of the Act.

The Heavy Metal Screening Test is a device because it is intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals. The Heavy Metal Screening Test, used to detect heavy metals in human urine, saliva and/or hair, is adulterated under section 501 (f)(1)(B) of the Act, 21 U.S.C. § 351(f)(1)(B), because an approved application for premarket approval (PMA) pursuant to section 515(a) of the Act, 21 U.S.C. § 360e(a), or an approved application for an investigational device exemption (IDE) under section 520(g) of the Act, 21 U.S.C. § 360j(g), are not in effect for it. The Heavy Metal Screen Test is also misbranded under section 502(o) of the Act, 21 U.S.C. § 352(o), in that it was manufactured, prepared, propagated, compounded or processed in an establishment not duly registered under section 510 of the Act, 21 U.S.C. § 360; not included in a list required by 510(j), 21 U.S.C. § 360(j); and notification or other information respecting the device was not provided to the FDA as required by section 510(k) of the Act, 21 U.S.C. § 360(k).
The issues and violations cited in this letter are not intended to be an all-inclusive statement of violations that exist in connection with your products. You are responsible for investigating and determining the causes of the violations identified above and for preventing their recurrence or the occurrence of other violations. It is your responsibility to ensure that your firm complies with all requirements of federal law and FDA regulations.

You should take prompt action to correct the violations cited in this letter. Failure to promptly correct these violations may result in legal action, without further notice, including, without limitation, seizure and injunction. Other federal agencies may take this Warning Letter into account when considering the award of contracts.
Within fifteen working days of receipt of this letter, please notify this office in writing of the specific steps that you have taken to correct violations. Include an explanation of each step being taken to prevent the recurrence of violations, as well as copies of related documentation. If you cannot complete corrective action within fifteen working days, state the reason for the delay and the time within which you will complete the correction. Furthermore, please advise this office what actions you will take to address product that you have already distributed. Additionally, if another firm
manufactures these products identified above, your reply should include the name and address of the manufacturer. If the firm from which you receive the products is not the manufacturer, please
include the name of your supplier in addition to the manufacturer. Address your reply to the Food and Drug Administration, 22201 23rd Drive Southeast, Bothell, Washington 98021-4421, Attention: Lisa M. Althar, Compliance Officer.
A description of the new drug approval process can be found on FDA’s internet website athttp://www.fda.gov/Drugs/DevelopmentApprovalProcess/default.htm. In addition, information regarding approval or clearance for devices is described athttp://www.fda.gov/cdrh/devadvice/3122.html. Any questions you may have regarding this process should be directed to the Food and Drug Administration, Division of Drug Information, Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, WO51-2201, Silver Spring, Maryland 20993-0002.

Sincerely,
/S/
Charles M. Breen
District Director

FDA Warning – AMAG Pharmaceuticals, Inc.

TRANSMITTED BY FACSIMILE

Brian J.G. Pereira, MD
President and Chief Executive Officer
AMAG Pharmaceuticals, Inc.
100 Hayden Avenue
Lexington, MA 02421
RE: NDA 020410, 022180
GastroMARK® (ferumoxsil, oral suspension)
Feraheme™ (ferumoxytol) Injection For Intravenous (IV) use
MACMIS #18355

WARNING LETTER

Dear Dr. Pereira:
As part of its routine monitoring and surveillance program, the Division of Drug Marketing, Advertising, and Communications (DDMAC) of the U.S. Food and Drug Administration (FDA) has reviewed AMAG Pharmaceuticals, Inc.’s (AMAG) webpages for its drug products, GastroMARK® (ferumoxsil, oral suspension) (GastroMARK)1 and Feraheme™ (ferumoxytol) Injection For Intravenous (IV) use (Feraheme).2 Both the GastroMARK and Feraheme webpages omit risks associated with the drug products; in addition, the GastroMARK webpage omits important information about the approved indication for GastroMARK, and both webpages misleadingly suggest unapproved new uses for the drugs. Thus, the webpages misbrand the drugs in violation of the Federal Food, Drug, and Cosmetic Act (the Act), 21 U.S.C. 352(a),(f)(1) & (n); 321(n), and FDA’s implementing regulations. See 21 CFR 201.100(c)(1); 201.128; 202.1(e)(3)(i);(e)(5) & (e)(6)(i). Furthermore, AMAG failed to submit a copy of the GastroMARK and Feraheme webpages to FDA under cover of Form FDA-2253 at the time of their initial publication, as required by 21 CFR 314.81(b)(3)(i).
These violations are concerning from a public health perspective because they suggest that GastroMARK is useful in a broader range of patients and conditions than has been demonstrated by substantial evidence or substantial clinical experience, and that GastroMARK and Feraheme are safer than has been demonstrated by substantial evidence or substantial clinical experience.

Background
GastroMARK
According to its FDA-approved product labeling (PI), GastroMARK is indicated as follows:
GastroMARK is indicated in adult patients for oral use with magnetic resonance imaging to enhance the delineation of the bowel to distinguish it from organs and tissues that are adjacent to the upper regions of the gastrointestinal tract.
GastroMARK’s usefulness in the lower gastrointestinal tract and retroperitoneal region is limited (by transit time and dilution).
GastroMARK is not recommended for iron supplementation.
GastroMARK is contraindicated in patients with known or suspected intestinal perforation or obstruction, and in patients with known allergy to its active or inactive ingredients.
The PI for GastroMARK includes the following Warnings:
The ingestion of GastroMARK may cause abdominal pain, diarrhea, nausea and vomiting. In 78/256 (30%) of patients and normal volunteers, gastrointestinal adverse events occurred within the first 2 hours after ingestion of GastroMARK. In 30 (12%), gastrointestinal events had their onset within 30 minutes. In 63/256 (24%), diarrhea occurred within 24 hours.
Vomiting can be associated with aspiration. Precautions should be taken to avoid aspiration.
The effects of GastroMARK on human peritoneal tissues are not known. In animal studies, intraperitoneal injection of GastroMARK was associated with a foreign body reaction that persisted for at least 30 days.
Additionally, the PI contains numerous Precautions, including the possibility of increased severity of nausea, vomiting, diarrhea, and abdominal cramping in patients who have these symptoms prior to GastroMARK administration; “This could confound the ability to distinguish adverse effects of GastroMARK from the signs and symptoms of obstruction or perforation, and from the pre-existing conditions.” In addition, studies have not been conducted in patients who have a current or recent history of hiatal hernia, esophageal reflux, nausea, vomiting, or abdominal pain; or to describe the effects of drugs that increase or decrease gastrointestinal transit time on the GastroMARK image quality or gastrointestinal adverse events. GastroMARK should be given with caution to patients who cannot tolerate large fluid shifts, who are on specific fluid intake requirements, and who have disorders associated with iron overload (e.g., hemosiderosis, chronic hemolytic anemia with frequent blood transfusions, or chronic iron replacement). Furthermore, the safety of GastroMARK in patients with inflammatory bowel disease has not been well studied.
Feraheme
According to its PI, “Feraheme™ (ferumoxytol) Injection is indicated for the treatment of iron deficiency anemia in adult patients with chronic kidney disease (CKD).”
Feraheme is contraindicated in patients with evidence of iron overload, known hypersensitivity to Feraheme or any of its components, and anemia not caused by iron deficiency.
Feraheme is associated with other serious risks. The PI includes Warnings and Precautions regarding the following (emphasis in original):
. . . HYPERSENSITIVITY REACTIONS
Feraheme may cause serious hypersensitivity reactions, including anaphylaxis and/or anaphylactoid reactions. In clinical studies, serious hypersensitivity reactions were reported in 0.2% (3/1,726) of subjects receiving Feraheme. Other adverse reactions potentially associated with hypersensitivity (e.g., pruritus, rash, urticaria or wheezing) were reported in 3.7% (63/1,726) of these subjects. Observe patients for signs and symptoms of hypersensitivity for at least 30 minutes following Feraheme injection and only administer the drug when personnel and therapies are readily available for the treatment of hypersensitivity reactions. . . .
. . . HYPOTENSION
Hypotension may follow Feraheme administration. In clinical studies, hypotension was reported in 1.9% (33/1,726) of subjects, including three patients with serious hypotensive reactions. Monitor patients for signs and symptoms of hypotension following Feraheme administration. . . .
. . . IRON OVERLOAD
Excessive therapy with parenteral iron can lead to excess storage of iron with the possibility of iatrogenic hemosiderosis. Regularly monitor the hematologic response during parenteral iron therapy. . .

In the 24 hours following administration of Feraheme, laboratory assays may overestimate serum iron and transferrin bound iron by also measuring the iron in the Feraheme complex.
. . . MAGNETIC RESONANCE (MR) IMAGING
Administration of Feraheme may transiently affect the diagnostic ability of MR imaging
. . . . Alteration of MR imaging studies may persist for up to 3 months following the last Feraheme dose. . . .
Feraheme will not interfere with X-ray, computed tomography (CT), positron emission tomography (PET), single photon emission tomography (SPECT), ultrasound or nuclear medicine imaging.

The most common adverse reactions reported in ≥2% of Feraheme-treated patients with CKD were nausea (3.1%), dizziness (2.6%), hypotension (2.5%), and peripheral edema (2.0%). Diarrhea (4.0%), constipation (2.1%), and hypertension (1.0%) have also been reported. In clinical trials, adverse reactions leading to treatment discontinuation in ≥2 Feraheme-treated patients included hypotension, infusion site swelling, increased serum ferritin level, chest pain, diarrhea, dizziness, ecchymosis, pruritus, chronic renal failure, and urticaria.
Omission of Risk/Indication Information
Promotional materials are misleading if they fail to reveal facts that are material in light of the representations made by the materials or with respect to consequences that may result from the use of the drug as recommended or suggested by the materials.
The webpages present numerous efficacy claims for GastroMARK and Feraheme, but fail to communicate any of the risks associated with the drugs (see Background section above). By omitting the most serious and frequently occurring risks associated with these drugs, the webpages misleadingly suggest that GastroMARK and Feraheme are safer than has been demonstrated and therefore place the public at risk. For example, the GastroMARK webpage omits the drug’s contraindication in patients with known or suspected intestinal perforation or obstruction. We note that there are links to “Download the GastroMARK® Package Insert” at the bottom of the GastroMARK webpage and to “Download the Feraheme Package Insert” buried in the second sentence of the Feraheme webpage. However, these links do not mitigate the complete omission of risk information from the GastroMARK and Feraheme webpages.
Furthermore, the GastroMARK webpage fails to present the complete indication for GastroMARK, including material limitations to the indication. The webpage includes the following claims:
GastroMARK® (ferumoxsil) is AMAG Pharmaceuticals’ oral gastrointestinal (GI) imaging agent for delineation of the bowel. . . . By more clearly identifying the intestinal loops, GastroMARK® enhances the ability to distinguish the bowel from adjacent tissues and organs in the upper gastrointestinal tract.
This presentation fails to include that GastroMARK is indicated only in adult patients, and that its usefulness in the lower gastrointestinal tract and retroperitoneal region is limited by transit time and dilution. The webpage also fails to reveal that GastroMARK is not recommended for iron supplementation.
Promotion of Unapproved Uses
The Feraheme webpage includes the following claims:
• “Feraheme is indicated for the treatment of iron deficiency anemia in adult patients with chronic kidney disease.”
• “Feraheme is being developed to treat iron deficiency anemia associated with other conditions and disease states including women with abnormal uterine bleeding, and patients with cancer and gastrointestinal diseases.”
• “Feraheme is also being developed as a diagnostic agent for vascular-enhanced magnetic resonance imaging to assess peripheral arterial disease. . . .”
The presentation of both approved and unapproved product information for Feraheme together in this manner is misleading because it implies that Feraheme is effective for unapproved uses. However, Feraheme is not approved to treat iron deficiency anemia in women with abnormal uterine bleeding, or in patients with cancer and gastrointestinal diseases. In addition, Feraheme is not approved as a diagnostic agent for vascular-enhanced magnetic resonance imaging for the detection of clinically significant arterial stenosis or occlusion in subjects with peripheral arterial disease.
Similarly, the GastroMARK webpage first presents the product’s U.S. indication (minus limitations), along with efficacy claims for the drug, but states near the bottom of the page that, “In Europe Gastromark® is approved for rectal administration to delineate the lower intestinal system” (emphasis added). This statement, presented within a webpage that appears to be targeted to a U.S. audience, is concerning, as it suggests to U.S. healthcare professionals that GastroMARK is effective for delineating the lower intestinal system and for rectal administration, when in fact, the drug is not approved for this use or method of administration in the U.S.; the U.S. PI for GastroMARK specifically states that “GastroMARK is indicated. . . for oral use. . . .” and that “GastroMARK’s usefulness in the lower gastrointestinal tract and retroperitoneal region is limited (by transit time and dilution).”
The above statements thus misbrand Feraheme and GastroMARK.
Failure to Submit on Form FDA-2253
FDA regulations require companies to submit any labeling or advertising devised for promotion of the drug product at the time of initial dissemination of the labeling and at the time of initial publication of the advertisement for a prescription drug product. Each submission is required to be accompanied by a completed transmittal Form FDA-2253 (Transmittal of Advertisements and Promotional Labeling for Drugs for Human Use) and is required to include a copy of the product’s current professional labeling. Copies of the GastroMARK and Feraheme webpages were not submitted to DDMAC under cover of Form FDA-2253 at the time of initial publication as required by 21 CFR 314.81(b)(3)(i).
Conclusion and Requested Action
For the reasons discussed above, the webpages misbrand GastroMARK and Feraheme in violation of the Act, 21 U.S.C. 352(a),(f)(1) & (n); 321(n), and FDA’s implementing regulations. See 21 CFR 201.100(c)(1); 201.128; 202.1(e)(3)(i);(e)(5) & (e)(6)(i). Furthermore, you failed to submit the webpages to FDA under cover of Form FDA-2253 at the time of their initial publication, as required by 21 CFR 314.81(b)(3)(i).
DDMAC requests that AMAG immediately cease the dissemination of violative promotional materials for GastroMARK and Feraheme, such as those described above. Please submit a written response to this letter on or before November 1, 2010, stating whether you intend to comply with this request, listing all promotional materials (with the 2253 submission date) for GastroMARK and Feraheme that contain violations such as those described above, and explaining your plan for discontinuing use of such violative materials. Because the violations described above are serious, we request, further, that your submission include a plan of action to disseminate truthful, non-misleading, and complete corrective messages about the issues discussed in this letter to the audience(s) that received the violative promotional materials. Please direct your response to me at the Food and Drug Administration, Center for Drug Evaluation and Research, Division of Drug Marketing, Advertising, and Communications, 5901-B Ammendale Road, Beltsville, MD 20705-1266, facsimile at 301-847-8444. In all future correspondence regarding this matter, please refer to MACMIS #18355 in addition to the NDA numbers. We remind you that only written communications are considered official.
The violations discussed in this letter do not necessarily constitute an exhaustive list. It is your responsibility to ensure that your promotional materials for GastroMARK and Feraheme comply with each applicable requirement of the Act and FDA implementing regulations.
Failure to correct the violations discussed above may result in FDA regulatory action, including seizure or injunction, without further notice.
Sincerely,
{See appended electronic signature page}
Thomas W. Abrams, R.Ph., M.B.A.
Director
Division of Drug Marketing,
Advertising, and Communications
CC: Russell D. Reed
Global Labeling Director
Mallinckrodt Inc.
675 McDonnell Boulevard
Hazelwood, MO 63042

1 GastroMARK webpage, at http://www.amagpharma.com/products/gastromark.php (last accessed October 18, 2010).
2 Feraheme webpage, at http://www.amagpharma.com/products/feraheme.php (last accessed October 18, 2010).
———————————————————————————————————
This is a representation of an electronic record that was signed electronically and this page is the manifestation of the electronic signature.
———————————————————————————————————
/s/
—————————————————-
THOMAS W ABRAMS
10/18/2010

WhoIs Fastmeds-now.com

Buying Prescription Drugs Online Scam Alert 1
May Be Dangerous
Says Drug Enforcement Administration


DEA Logo - Buying Proscription Drugs

Click Here
National Association of Boards of Pharmacy (NABP)

Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Behind The Online Pharmacy

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.

Department of Justice – Ryan Haight Act
Read More Health Canada


These people are unbelievable.  I’ve been called twice today, five times in the last week.  I also am on the FTC Do Not Call Registry.  What the hell is wrong with this company?

By the way, the website guilty of this is fastmeds-now.com.  Their number is at 1-866-545-7099.  I suggest we all call them and take up their time, too.

Maybe we should all go order something from their site, and then return it.

Address lookup
canonical name fastmeds-now.com
aliases
addresses 92.52.81.96
Domain Whois record

Queried whois.internic.net with “dom fastmeds-now.com”…

Domain Name: WWW.FASTMEDS-NOW.COM
Registrar: ABSYSTEMS INC
Whois Server: whois.yournamemonkey.com
Referral URL: http://www.yournamemonkey.com
Name Server: NS1.FASTMEDS-NOW.COM
Name Server: NS2.FASTMEDS-NOW.COM
Status: ok
Updated Date: 26-mar-2010
Creation Date: 25-mar-2009
Expiration Date: 25-mar-2011

Last update of whois database: Sat, 02 Oct 2010 07:25:10 UTC
Queried whois.yournamemonkey.com with “fastmeds-now.com”

——-
Domain name: fastmeds-now.com

Registrant Contact:
Dami Waryoba, damiw1975@fastmeds-now.com
1811 E Farnkford Rd 2104
Carrollton, TX 75007
US
+1.2147312290

Administrative Contact:
Dami Waryoba, damiw1975@fastmeds-now.com
1811 E Farnkford Rd 2104
Carrollton, TX 75007
US
+1.2147312290

Billing Contact:
Dami Waryoba, damiw1975@fastmeds-now.com
1811 E Farnkford Rd 2104
Carrollton, TX 75007
US
+1.2147312290

Technical Contact:
Dami Waryoba, damiw1975@fastmeds-now.com
1811 E Farnkford Rd 2104
Carrollton, TX 75007
US
+1.2147312290

Status:
Active

Name Servers:
NS1.FASTMEDS-NOW.COM
NS2.FASTMEDS-NOW.COM

Creation date: 26 Mar 2009 11:57:09
Expiration date: 26 Mar 2011 02:40:23
——-
Network Whois record

Queried whois.ripe.net with “-B 92.52.81.96″…

% Information related to ‘92.52.81.96 – 92.52.81.127’

inetnum: 92.52.81.96 – 92.52.81.127
netname: RSPC-UK-David-Martin—Company
descr: David Martin – Company IP Space
country: GB
admin-c: IA247-RIPE
tech-c: IA247-RIPE
status: ASSIGNED PA
notify: hostmaster@rackspace.com
mnt-by: RSPC-MNT
changed: hostmaster@rackspace.com 20100809
source: RIPE

person: IP Admin
address: Rackspace Managed Hosting
112 E. Pecan St. Suite 600
San Antonio, Texas 78205
phone: +1 210 892 4000
fax-no: +1 210 892 4329
e-mail: ipadmin@rackspace.com
nic-hdl: IA247-RIPE
remarks: ### Rackspace Abuse Department
remarks: ### Please send any complaints to the following:
remarks: ### abuse@rackspace.com
notify: ipadmin@rackspace.com
mnt-by: RSPC-MNT
changed: ipadmin@rackspace.com 20021021
source: RIPE

% Information related to ‘92.52.64.0/18AS15395’

route: 92.52.64.0/18
descr: Route entry for Rackspace
origin: AS15395
mnt-by: RSPC-MNT
changed: hostmaster@rackspace.com 20080129
source: RIPE
DNS records

DNS query for 96.81.52.92.in-addr.arpa returned an error from the server: NameError

name class type data time to live
fastmeds-now.com IN SOA
server: ns1.fastmeds-now.com
email: hostmaster.fastmeds-now.com
serial: 1238032604
refresh: 7200
retry: 3600
expire: 604800
minimum ttl: 3600
3600s (01:00:00)
fastmeds-now.com IN NS ns1.fastmeds-now.com 3600s (01:00:00)
fastmeds-now.com IN MX
preference: 10
exchange: ns1.fastmeds-now.com
3600s (01:00:00)
fastmeds-now.com IN A 92.52.81.96 3600s (01:00:00)
— end —

Pharmacy Spam – refillonweb.net – greatness4u.net

Buying Prescription Drugs Online Scam Alert 1
May Be Dangerous
Says Drug Enforcement Administration

DEA Logo - Buying Proscription Drugs

Click Here
National Association of Boards of Pharmacy (NABP)

Warning

“The Canadian Pharmacy, Canadian/European Pharmacy”, “Canadian Healthcare” and “US Drugstore” are brands of one of the most disgusting illegal online pharmacy group well organized CRIMINAL OPERATION of all times. “GREED” is the driving force behind this operation. Don’t let them fool you. They will never send you any genuine drugs. If they ever send anything at all, it may consist of literally anything from sugar to wall plaster, and they certainly don’t care that you will endanger your health by taking those dangerous counterfeit drugs.

Behind The Online Pharmacy

Today a shadowy, transnational network of illicit drug manufacturers, traders, doctors, Web site operators, spammers and criminals makes up the online pharmacy world.

Buying Medication Online Can Be Safe

There are many options out there when it comes to buying medication online. We have looked at websites after websites. Some sites feature offshore pharmacies that do not require a prior prescription. Others feature licensed pharmacies that do require a prescription from your doctor.
Before making a purchase that can effect your health, we strongly recommend that you consult your physician & DO NOT self-medicate. Ordering medication online can be a safe, money-saving experience. When done through licensed online pharmacies that require a prescription, you can be assured that the medication you get is exactly what you need to treat your ailments.

Also See ThreatChaos

Department of Justice – Ryan Haight Act


RxMedications are available at your Fingertips!
No doctor or RxNeeded!
Browse Our Selection Today! -> http://greatness4u.net

All of your Favorite Rx~Medications are at your Fingertips!
NoDoctor_or_RX_needed!
Browse Our Website Today! -> http://refillonweb.net

Address lookup

canonical name greatness4u.net.
aliases
addresses 116.123.221.214

Domain Whois record

Queried whois.internic.net with “dom greatness4u.net”…
Domain Name: GREATNESS4U.NET
Registrar: CHINA SPRINGBOARD INC.
Whois Server: whois.namerich.cn
Referral URL: http://www.namerich.cn
Name Server: NS1.DOGMENS.COM
Name Server: NS2.DOGMENS.COM
Name Server: NS3.DOGMENS.COM
Name Server: NS4.DOGMENS.COM
Status: clientDeleteProhibited
Status: clientTransferProhibited
Updated Date: 01-jan-2010
Creation Date: 29-oct-2009
Expiration Date: 29-oct-2010

Last update of whois database: Sun, 10 Jan 2010 18:12:26 UTC <<<

Queried whois.namerich.cn with “greatness4u.net”…
DomainName : greatness4u.net

RSP: China Springboard Inc.
URL: http://www.namerich.cn

Name Server: NS2.DOGMENS.COM
Name Server: NS4.DOGMENS.COM
Name Server: NS1.DOGMENS.COM
Name Server: NS3.DOGMENS.COM
Status: clientTransferProhibited
Status: clientDeleteProhibited
Creation Date: 2009-10-30
Expiration Date: 2010-10-30
Last Update Date: 2010-01-02

Registrant Name: zhang cheng san
Registrant Organization: zhao cheng san
Registrant Address: yangzhoushinanminglu56hao
Registrant City: yangzhou
Registrant Province/State: JiangSu
Registrant Country Code: CN
Registrant Postal Code: 123577
Registrant Phone Number: +86.02456983265
Registrant Fax: +86.02456983265
Registrant Email: fgretdfsd@126.com

Administrative Name: zhang cheng san
Administrative Organization: zhao cheng san
Administrative Address: yangzhoushinanminglu56hao
Administrative City: yangzhou
Administrative Province/State: JiangSu
Administrative Country Code: CN
Administrative Postal Code: 123577
Administrative Phone Number: +86.02456983265
Administrative Fax: +86.02456983265
Administrative Email: fgretdfsd@126.com

Billing Name: zhang cheng san
Billing Organization: zhao cheng san
Billing Address: yangzhoushinanminglu56hao
Billing City: yangzhou
Billing Province/State: JiangSu
Billing Country Code: CN
Billing Postal Code: 123577
Billing Phone Number: +86.02456983265
Billing Fax: +86.02456983265
Billing Email: fgretdfsd@126.com

Technical Name: zhang cheng san
Technical Organization: zhao cheng san
Technical Address: yangzhoushinanminglu56hao
Technical City: yangzhou
Technical Province/State: JiangSu
Technical Country Code: CN
Technical Postal Code: 123577
Technical Phone Number: +86.02456983265
Technical Fax: +86.02456983265
Technical Email: fgretdfsd@126.com

; Please register your domains at
; http://www.namerich.cn

Network Whois record

Queried whois.apnic.net with “116.123.221.214”…
inetnum: 116.120.0.0 – 116.127.255.255
netname: HANANET
descr: Hanaro Telecom
descr: Shindongah Bldg, 43, Taepyeongno2-ga,
descr: Jung-gu, Seoul
descr: ***********************************
descr: Allocated to KRNIC Member.
descr: If you would like to find assignment
descr: information in detail please refer to
descr: the KRNIC Whois Database at:
descr: http://whois.nic.or.kr/english/index.htm
descr: ***********************************
country: KR
admin-c: HL196-AP
tech-c: JK250-AP
status: Allocated Portable
remarks: http://www.hanaro.com
mnt-by: MNT-KRNIC-AP
mnt-lower: MNT-KRNIC-AP
changed: hm-changed@apnic.net 20070521
source: APNIC

person: Han Lee
nic-hdl: HL196-AP
e-mail: ip-adm@hanaro.com
address: 726-1, Janghang2-dong, Goyang-si, Ilsan-gu, Seoul
phone: +82-2-106
fax-no: +82-2-6266-6483
country: KR
changed: hostmaster@nic.or.kr 20040326
mnt-by: MNT-KRNIC-AP
source: APNIC

person: Jinyoung Kim
nic-hdl: JK250-AP
e-mail: ip-adm@hanaro.com
address: 726-1, Janghang2-dong, Goyang-si, Ilsan-gu, Seoul
phone: +82-2-106
fax-no: +82-2-6266-6483
country: KR
changed: hostmaster@nic.or.kr 20040326
mnt-by: MNT-KRNIC-AP
source: APNIC

DNS records

DNS query for 214.221.123.116.in-addr.arpa returned an error from the server: NameError

name class type data time to live
greatness4u.net IN SOA
server: ns1.domain.com
email: admin.domain.com
serial: 1
refresh: 300
retry: 300
expire: 300
minimum ttl: 2700
2700s (00:45:00)
greatness4u.net IN A 116.123.221.214 2700s (00:45:00)
greatness4u.net IN NS ns1.greatness4u.net 2700s (00:45:00)
greatness4u.net IN NS ns2.greatness4u.net 2700s (00:45:00)
greatness4u.net IN NS ns3.greatness4u.net 2700s (00:45:00)
greatness4u.net IN NS ns4.greatness4u.net 2700s (00:45:00)

— end —

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Changsha, Hunan, China

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