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U.S. Department of Health and Human Services

Drugs

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Maitake Mushroom, Memory Formula #2, Mistletoe (European), Kidney/Bladder,Omega 3 Flaxs Seed Oil - High Lignan, and Fringe Tree

 

April 8, 2004

CERTIFIED MAIL
RETURN RECEIPT REQUESTED

Janet Dillon
American Health & Herbs
1313 Main Street
Philomath, Oregon 97370

Ref. No. CL-03-HFS-810-90

Dear Ms. Dillon:

This is to advise you that the Food and Drug Administration (FDA) has reviewed your web site at the Internet address http://www.healthherbs.com and has determined that the products “Maitake Mushroom,” “Memory Formula #2,” “Mistletoe (European),” “Kidney/Bladder,” “Omega 3 Flaxs Seed Oil – High Lignan,” and “Fringe Tree” are promoted for conditions that cause the products to be drugs under section 201(g)(1) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 USC 321(g)(1)]. The therapeutic claims on your web site establish that these 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 web site include:

Maitake Mushroom
“For strengthening the immune system to fight disease and heal.”

Memory Formula #2
“Helps with Meniere’s Syndrome . Use for …disorders which may result in memory loss, such as Alzheimer’s.”

Mistletoe (European)
“Lowers blood pressure ...” “Helps with arteriosclerosis and tumors.”

Kidney/Bladder
“[H]elp fight infection of the kidneys and bladder.”

Omega 3 Flax Seed Oil – High Lignan
“Reduces symptoms of … allergy/asthma …beneficial against cancer and diabetes.”

Fringe Tree
“[G]radually dissolves gallstones and prevents their formation. Also for jaundice and other liver disorders.”

Furthermore, FDA has no information that your products are generally recognized as safe and effective for the above referenced conditions and therefore, the products may also be
“new drugs” under section 201(p) of the Act [21 USC 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 USC 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.

FDA is aware that Internet distributors may not know that the products they offer are regulated as drugs or that these drugs are not in compliance with the law. Many of these products may be legally marketed as dietary supplements or as cosmetics if therapeutic claims are removed from the promotional materials and the products otherwise comply with all applicable provisions of the Act and FDA regulations.

Under the Act, as amended by the Dietary Supplement Health and Education Act (DSHEA), dietary supplements may be legally marketed with truthful and non-misleading claims to affect the structure or function of the body (structure/function claims), if certain conditions are met. However, claims that dietary supplements are intended to prevent, diagnose, mitigate, treat, or cure disease (disease claims), excepting health claims authorized for use by FDA, cause the products to be drugs. The intended use of a product may be established through product labels and labeling, catalogs, brochures, audio and videotapes, Internet sites, or other circumstances surrounding the distribution of the product. FDA has published a final rule intended to clarify the distinction between structure/function claims and disease claims. This document is available on the Internet at http://vm.cfsan.fda.gov/~lrd/fr000106.html (codified at 21 C.F.R. 101.93(g)).

In addition, only products that are intended for ingestion may be lawfully marketed as dietary supplements. Topical products and products intended to enter into the body directly through the skin or mucosal tissues, such as transdermal or sublingual products, are not dietary supplements. For these products, both disease and structure/function claims may cause them to be new drugs.

Certain over-the-counter drugs are not new drugs and may be legally marketed without prior approval from FDA. Additional information is available in Title 21 of the Code of Federal Regulations (21 CFR) Parts 310 and 330-358, which contain FDA's regulations on over-the-counter drugs.

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

If you need additional information or have questions concerning any products distributed through your web site, please contact FDA. You may reach FDA electronically (e-mail) at APope@CFSAN.FDA.GOV, or you may respond in writing to Angela F. Pope, Compliance Officer, Food and Drug Administration, Division of Compliance and Enforcement, 5100 Paint Branch Parkway, College Park, Maryland 20740-3835. If you have any questions concerning any issue in this letter, please contact Ms. Pope at (301) 436-2375.

Sincerely yours,
/s/


Susan J. Walker, M.D.
Director
Division of Dietary Supplement Programs
Office of Nutritional Products, Labeling
and Dietary Supplements
Center for Food Safety
and Applied Nutrition