Inspections, Compliance, Enforcement, and Criminal Investigations
Heba Laboratories, LLC 09-Nov-05
Department of Health and Human Services
| Public Health Service |
Food and Drug Administration
|Center for Food Safety and Applied Nutrition, HFS-607 |
5100 Paint Branch Parkway
College Park, MD 20740
RETURN RECEIPT REQUESTED
November 9, 2005
Heba™ Laboratories, LLC
460 Smith Street, Suite # B2
Middletown, CT 06457
This is to advise you that the Food and Drug Administration (FDA) has reviewed your web site at the Internet address http://www.hebamedicine.com and has determined that the product HebaSoy™ 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)(B)]. The therapeutic claims on your web site 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 this product with these claims violates the Act.
Examples of some of the claims observed on your web site include:
“HebaSoy™- A woman’s best defense against cancer, heart disease…”
“[R]educes the risk of breast and prostate cancer, decreases risk of atherosclerosis…helps with rheumatoid arthritis… and osteoporosis.”
“By protecting against heart disease, osteoporosis, atherosclerosis and breast/prostate cancer, the daidzein and genistein in HebaSoy™….”
“Genistein [an ingredient in HebaSoy™] also has been found to block an enzyme that stimulates the growth of cancer cells.”
Furthermore, your product is not generally recognized as safe and effective for the above referenced conditions and therefore, the product is also 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. Your HebaSoy™ is also misbranded within the meaning of section 502(f)(1) of the Act, in that the labeling for this drug fails to bear adequate directions for use [21 U.S.C. § 352(f)(1)].
This letter is not an all-inclusive review of your website and the products that your firm markets. It is your responsibility to ensure that all products marketed by your firm comply with the Act and its implementing regulations.
The Act authorizes injunctions against manufacturers and distributors of illegal products and seizure of such products [21 U.S.C. §§ 332 and 334]. You should take prompt action to correct the violations identified in this letter and any other violations of the Act. Failure to do so may result in enforcement action without further notice.
Furthermore, you should be aware that laws enforced by the Federal Trade Commission (FTC) govern claims made in advertising, including print, broadcast, websites, and other electronic media. The FTC Act, 15 U.S.C. § 41 et seq., prohibits unfair or deceptive acts and practices, including false and unsubstantiated advertising claims. It is against the law to make health claims without substantiation or to overstate the health benefits of the products you promote. Be aware that product claims can be communicated to consumers in a variety of ways, including product name, website name, product testimonials, endorsements, or use of metatags.
Please advise 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. 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 reply should be addressed to Quyen Tien, Compliance Officer, at the above letterhead address.
Joseph R. Baca
Office of Compliance
Center for Food Safety and Applied Nutrition