8/21/2023 0 Comments Caffeine supplementManufacturers of liquid caffeinated products may choose to label these products as beverages or dietary supplements, but there are requirements for both, and that decision has regulatory consequences for the manufacturer. ![]() It is incorrect to say that energy drinks labeled as dietary supplements are beyond FDA’s reach for evaluation of their safety, or that caffeine-containing products labeled as dietary supplements are less regulated than conventional beverages.FDA also has ample authority under the Food, Drug, and Cosmetic Act (FDCA) to demand recalls, to seize products, to detain imports or to impose civil and criminal penalties for products that are adulterated, misbranded, or that pose a safety risk to consumers.FDA has the authority to review dietary supplement labeling and the ability to remove a dietary supplement from the market if it poses an “imminent hazard” or “significant or unreasonable risk of injury or illness.” 1 Dietary supplements are subject to postmarket surveillance through mandatory serious adverse event reporting-a requirement that does not apply to conventional foods and beverages. FDA imposes Good Manufacturing Practices (GMP) regulations on supplements that are more strict than those for other food.International Trade & Market DevelopmentĪs a category of food, all dietary supplements are subject to comprehensive, robust regulation.Economic Impact of the Dietary Supplement Industry.Dietary Supplement Health & Education Act (DSHEA). ![]()
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |