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Microcap & Penny Stocks : Amazon Natural (AZNT) -- Ignore unavailable to you. Want to Upgrade?


To: Arcane Lore who wrote (5675)9/16/1998 12:19:00 AM
From: hawkeye  Read Replies (1) | Respond to of 26163
 
Arcane (not Anthony), The FDA prohibition you refer to ONLY APPLIES TO THE LABEL ON THE PRODUCT BOTTLE! The AZNT website only recommends (through an
ailment index with links) certain of its products for cancer. Nowhere in the links you provide does
AZNT itself claim that the product "CURES' cancer.
For Pau D'aco the web site says the product has "been been used...with great success" to treat
tumors and that "it has been proven to inhibit"
tumors. (This is true. hawkeye can provide links.)
For Hydrasis, AZNT references findings of third parties. The DSHEA specifically allows the
dissemination of third-party studies about dietary
supplements.



To: Arcane Lore who wrote (5675)9/16/1998 12:24:00 AM
From: s martin  Read Replies (1) | Respond to of 26163
 
>>Incidentally, even though the name "Astley Paston Cooper" sounds bogus, there really was an English surgeon by that name (born 1768, died 1841). Not that the FDA would regard the mention of an undocumented endorsement by a 19th century surgeon as adequate evidence of safety and efficacy. <<

If you hadn't filled us in Pugs would be claiming that Astley and Loricchio were collaborators.... Catchy name Astley, wonder who came up with that one ? Sure would like to know who writes all this tripe for AZNT. <G>



To: Arcane Lore who wrote (5675)9/18/1998 12:03:00 AM
From: Arcane Lore  Read Replies (1) | Respond to of 26163
 
Spanish fly, anyone?

From an FDA article titled "Looking for a Libido Lift? The Facts About Aphrodisiacs":

An aphrodisiac is a food, drink, drug, scent, or device that, promoters claim, can arouse or increase sexual desire, or libido. A broader definition includes products that improve sexual performance. Named after Aphrodite, the Greek goddess of sexual love and beauty, the list of supposed sexual stimulants includes anchovies and adrenaline, licorice and lard, scallops and Spanish fly, and hundreds of other items.

According to the Food and Drug Administration, the reputed sexual effects of so-called aphrodisiacs are based in folklore, not fact. In 1989, the agency declared that there is no scientific proof that any over-the-counter aphrodisiacs work to treat sexual dysfunction.

... FDA sends warning letters to companies that make aphrodisiac claims, stating that the agency may take further regulatory action if the violations continue. "In the health fraud area, when they get a warning letter, most people take their profits and run," says Joel Aronson, director of FDA's division of nontraditional drugs. "They don't want to get into a legal battle with the agency because it could involve protracted, expensive litigation."


vm.cfsan.fda.gov

Fraudulent sexual aids are number five on FDA's list of top health frauds:
fda.gov

Currently AZNT has a number of products it specifically describes with the term 'aphrodisiac'. For example:

Catuaba is a very strong aphrodisiac for both men and women of all ages.
amazon-treasures.com

It's also available as a tea apparently with the same aphrodisiac properties:
amazon-treasures.com
=====
Marapuama Tea is an aphrodisiac and will sexual impotency when taken in conjunction with Catuaba and Guarana Selva.
amazon-treasures.com

This one is also available in a non-tea form. While AZNT doesn't use the term 'aphrodisiac' for this form, they do note that it combats sexual impotency.
amazon-treasures.com
=====
According to the following page, fafia is also an aphrodisiac:

amazon-treasures.com

The web page for fafia makes due with the phrase: Sexual energies will be restored and a new state of health and fitness will be achieved for all type of activities and pleasure. amazon-treasures.com
=====
There are also several more that would appear to fall under FDA's broader definition of aphrodisiac:

amazon-treasures.com
amazon-treasures.com
amazon-treasures.com
amazon-treasures.com



To: Arcane Lore who wrote (5675)11/18/1998 10:00:00 PM
From: Arcane Lore  Read Replies (1) | Respond to of 26163
 
F.T.C. Guidelines Restrict Ad Claims for Supplements

For the first time, the Federal Trade Commission is issuing advertising guidelines aimed specifically at the nation's booming dietary supplement industry.

The guidelines are the commission's second action within a week on claims by the industry, which earned nearly $12 billion in 1997 and is growing at about 20 percent a year. Last week the commission e-mailed warnings to 1,200 Internet sites that it said had made "incredible claims" for drugs, devices and dietary supplements, including herbal remedies that purported to ward off AIDS or cure cancer. ...


nytimes.com
(Free registration required)

I wonder if AZNT has gotten any interesting email recently?

Guidelines set advertising parameters for booming industry

Manufacturers of dietary supplements must not only back up the explicit claims they make about their products, but also the benefits they imply through advertising, according to a set of government guidelines being released today. ...


boston.com



To: Arcane Lore who wrote (5675)11/22/1998 4:25:00 PM
From: Arcane Lore  Read Replies (1) | Respond to of 26163
 
<off topic?>


DEPARTMENT OF HEALTH & HUMAN SERVICES

Public Health Service

Food and Drug Administration
<snip>

HAND-DELIVERED

WARNING LETTER

<snip>

***, President
***

Dear Mr. ***:

During an inspection of your firm on ***, FDA Investigator Alfred L. Chester determined that you market and distribute Cat's Claw and Nu-Green which are being promoted to treat disease conditions.

We regard your promotional brochures as labeling which make therapeutic claims for these products. These claims cause these products to be drugs within the meaning of section 201(g) of the Federal Food, Drug, and Cosmetic Act (the Act). These products are "new drugs" within the meaning of section 201(p) of the Act and, therefore, may not be marketed in the United States without approved new drug applications under section 505 of the Act.

Your promotional material describes "Cats Claw" as an herb used "in the treatment of arthritis, gastritis, certain cancers, and other known epidemic diseases". Your promotional material also offers "Cats Claw" for such serious conditions as "Chrone's [sic] disease, diverticulitis, recurring ulcers, and other intestinal conditions. The material further states that "Cats Claw" "combats inflammation and tumor growth."

In addition, the claims made for your product "Nu-Green" include "an immunization effect against many dietary carcinogens."

These claims cause the above referenced product to be misbranded within the meaning of section 502(a) because the labeling is false and misleading as it suggests that the products are safe and effective for their intended uses when, in fact, this has not been established, and section 502(f)(1) because the labeling fails to bear adequate directions for use.

This letter is not intended to be an all inclusive review of all labeling and products your firm markets. It is your responsibility to ensure that all products marketed by your firm are in compliance with the Act and its implementing regulations.

We request that you take prompt action to correct these violations. Failure to promptly correct violations may result in enforcement action being initiated by the Food and Drug Administration without further notice. The Federal Food, Drug, and Cosmetic Act provides for the seizure of illegal products and for injunction against the manufacturer and/or distributor of illegal products.

Please notify this office in writing within fifteen (15) working days of receipt of this letter as to the specific steps you have taken to correct the stated violations. You should also include an explanation of each step being taken to identify and make corrections to assure that similar violations will not recur. If corrective action cannot be completed within 15 working days, state the reason for the delay and the time within which the corrections will be implemented.

Your reply should be sent to the attention of <snip>
Sincerely,

/s/ Douglas D. Tolen
<snip>



To: Arcane Lore who wrote (5675)6/24/1999 1:08:00 PM
From: Arcane Lore  Respond to of 26163
 
"Operation Cure.all" Targets Internet Health Fraud

FTC Law Enforcement and Consumer Education Campaign Focuses on Stopping the Quacks and Supplying Consumers with Quality Information

Internet health fraud is the target of a comprehensive law enforcement and consumer education campaign announced today by the Federal Trade Commission at a press conference in Washington, D.C. The campaign, "Operation Cure.All," uses the Internet both as a law enforcement tool to stop bogus claims for products and treatments touted as cures for various diseases and as a communication tool to provide consumers with good quality health information. Four cases that resulted from the agency's "Health Claims Surf Day" were part of today's announcement. The companies settled FTC charges that the four web sites made deceptive and unsubstantiated health claims concerning "miracle cures" for serious illnesses: cancer, arthritis, heart disease, and liver disease, among others. Also unveiled at the press conference were valuable resources for consumers to use to obtain reliable health information on the Web.

"Quality, not quackery is the focus of our new campaign, "Operation Cure.All," said Jodie Bernstein, Director of the FTC's Bureau of Consumer Protection. "As consumers become more assertive about making their own health care decisions, the Internet offers a powerful tool for finding health information. Our survey of the web sites found that too many make deceptive, unproven and fraudulent claims. Miracle cures, once thought to be laughed out of existence, have found a new medium. Consumers now spend millions on unproven, deceptively marketed products on the Web. Our law enforcement efforts will continue to focus on deceptive and unproven claims. But limited resources cannot keep up with the proliferation of web sites promoting fraudulent products. Consumers must be provided with reliable resources so that they can use the Internet to find the support and health care information they need."

...

At the press conference, Bernstein outlined the charges in the four cases, gave the results of "Health Claims Surf Days," which the agency conducted with public health, consumer protection and information agencies from 25 countries, including the United States, Canada, and Mexico, and introduced two new FTC Consumer Alerts, titled "Fraudulent Health Claims: Don't Be Fooled" and "Virtual 'Treatments' Can Be Real-World Deceptions."

...

The FTC conducted two Health Claim Surf Days, one in 1997 and the other in 1998. The surf days identified approximately 800 World Wide Web sites and numerous Usenet newsgroups that contain questionable promotions for products or services purporting to help cure, treat or prevent six diseases: heart disease, cancer, AIDS, diabetes, arthritis, and multiple sclerosis. After each Surf Day, web sites were sent e-mail messages, alerting them that their claims require scientific substantiation and that disseminating false or unsubstantiated claims violates federal law. Following the e-mail, FTC staff surveyed a representative sample of the 1998 sites and found that 28 percent of the sites had either removed their claims or had been taken down. Bernstein said that the agency is very encouraged by the fact that over a hundred sites making questionable claims voluntarily cleaned up their act, but warned that the agency will continue to monitor the Web for fraud and deception and bring law enforcement cases as appropriate.

In the four FTC cases announced today, the companies were charged with making unsubstantiated health claims for products advertised on the Internet. The companies agreed to settle the charges and the proposed settlement agreements were announced today for public comment.

According to the agency, John Sneed and Melinda Sneed d/b/a Arthritis Pain Care Center (APCC) marketed CMO, purportedly a fatty acid derived from beef tallow, to distributors and consumers. APCC claimed that CMO cures most forms of arthritis by permanently modifying the immune system, and that the product is beneficial in treating numerous other diseases. The complaint alleges that APCC's efficacy claims are unsubstantiated and that the claims about certain scientific studies, including studies at the National Institutes of Health, are false. The proposed settlement would resolve the charges by prohibiting APCC from making unsubstantiated claims for CMO. The company also would be prevented from making unsubstantiated health claims for any food, drug, dietary supplement or program and from misrepresenting the results of any tests or research.

Body Systems Technology, Inc. (BST) sells to consumers shark cartilage capsules as well as capsules and liquid containing a Peruvian plant derivative, Cat's Claw, the agency charged. The company promoted them as effective treatments for cancer, HIV/AIDS, and arthritis, and represented to consumers that scientific studies established their efficacy. In fact, according to the FTC, the claims are unsubstantiated. The proposed consent order would prohibit similar unsubstantiated claims for any product or program and also would bar BST from making unsubstantiated health claims for any food, drug, dietary supplement or program. Additionally, the proposed order would require BST to identify, notify, and make refunds to all purchasers of these products during a proscribed period of time, the agency said.

Magnetic Therapeutic Technologies, Inc. and Jim B. Richardson (MTT) promote magnetic therapy devices, using testimonials to help extol their purported ability to treat and alleviate a multitude of medical problems and diseases, including various types of cancer and high blood pressure. According to the FTC's complaint, MTT made unsubstantiated claims that its magnetic therapy products are effective in treating various cancers, HIV and other diseases and health conditions. The proposed consent order would prohibit MTT from making similar unsubstantiated claims for magnetic therapy products and other unsubstantiated claims about health benefits, performance or efficacy of any product or program.

Pain Stops Here! Inc. and Sande R. Caplin (PSH), also promoted magnetic therapy devices and made disease treatment claims for its devices. This company operates in a similar manner as MTT, the FTC said. PSH markets magnetic therapy devices as effective in treating a variety of ailments, including cancer, liver disease, and arthritis. The complaint challenges ten claims as unsubstantiated. The proposed consent order would prohibit PSH from making similar unsubstantiated efficacy claims for magnetic therapy products, as well as any other unsubstantiated claims about the performance, safety, efficacy, or health benefits of any product or program. It also would prohibit PSH from misrepresenting the results of any scientific studies or research.

Bernstein offered consumers the following tips for evaluating any health claim. She said if it sounds too good to be true, it probably is. She also said to be on the lookout for the typical phrases and marketing techniques fraudulent promoters use to deceive consumers.

** The product is advertised as a quick and effective cure-all for a wide range of ailments.

** The promoters use words like scientific breakthrough, miraculous cure, exclusive product, secret ingredient or ancient remedy.

** The text is written in "medicalese" - impressive-sounding terminology to disguise a lack of good science.

** The promoter claims the government, the medical profession or research scientists have conspired to suppress the product.

** The advertisement includes undocumented case histories claiming amazing results.

** The product is advertised as available from only one source.

...

ftc.gov