Consumer Health Digest #17-47

Your Weekly Update of News and Reviews
December 24, 2017

Consumer Health Digest is a free weekly e-mail newsletter edited by Stephen Barrett, M.D., with help from William M. London, Ed.D., M.P.H. It summarizes scientific reports; legislative developments; enforcement actions; news reports; Web site evaluations; recommended and nonrecommended books; and other information relevant to consumer protection and consumer decision-making. Its primary focus is on health, but occasionally it includes non-health scams and practical tips.

FDA proposes new homeopathic product regulations. The U.S. Food and Drug Administration has proposed what it calls "risk-based guidelines" that give enforcement priority to homeopathic products with the greatest potential risk to patients. [FDA proposes new, risk-based enforcement priorities to protect consumers from potentially harmful, unproven homeopathic drugs. FDA news release, Dec 18, 2017] The FDA intends to focus on:

Although homeopathic products have no proven effectiveness and their theoretical basis is senseless, a complete ban is not politically feasible. [Barrett S. Homeopathy: The ultimate fake. Quackwatch, Aug 25, 2016] However, the FDA can easily limit their marketing to single-ingredient products that strictly comply with the Homeopathic Pharmacopeia. No health claims should be permitted for homeopathic products unless they are approved through the FDA's standard drug approval process. The only statements that should be permitted in labeling or advertising are the chemical name, the dilution, and that fact that the product is homeopathic. Products consistent with the Pharmacopeia could still be marketed, so consumers who want homeopathic products could still obtain them. But unapproved health claims—including implied claims in product names—should be banned. If you agree with this suggestion, please read Dr. Barrett's full explanation and post a comment in your own words to the FDA comments page.

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This page was posted on December 25, 2017.