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Dick Durbin Reintroduces Dietary Supplement Listing Act
On Jan. 15, U.S. Senator Dick Durbin (D-IL) reintroduced the Dietary Supplement Listing Act, which would require dietary supplement manufacturers to register their products with the U.S. Food and Drug Administration (FDA). According to Durbin, the law would require companies to provide FDA with critical information about their products including product names, a list of ...
FDA Issues Final Guidance for Industry Addressing Food Allergen Labeling Requirements
The U.S. Food and Drug Administration (FDA) announced the availability of the Final Guidance for Industry: Questions and Answers Regarding Food Allergens, Including the Food Allergen Labeling Requirements of the Federal Food, Drug and Cosmetic Act (Edition 5). This final guidance is replacing all previously issued draft and final guidances by FDA concerning allergen labeling. ...
NPA Comments On New York Attorney General’s Subpoenas
Natural Products Association (NPA) CEO and Executive Director Daniel Fabricant, PhD, commented on the subpoenas issued by New York Attorney General Eric T. Schneiderman to four major retailers ordering evidence to back up their label claims. “The attorney general is using these subpoenas as a misdirection, removing focus from the fact that he still has ...
FDA Youth Outreach Campaign A Healthy Hit
Read the Label! Catching the attention of kids and families with its instructive slogan, the U.S. Food and Drug Administration (FDA) Read the Label Youth Outreach Campaign continues to grow strong since its 2007 inception. This comprehensive program from FDA has evolved into a nationwide grassroots initiative, the agency reports, adding how through this hands-on ...
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