You may have noticed that many marketers nowadays claim that their products are “FDA approved,” but how can you really be sure?
The U.S. Food and Drug Administration (FDA) is responsible for protecting public health by monitoring human prescription drugs and biologics, medical devices, animal drugs, tobacco products, food, electronic products that emit radiation, and cosmetics.
Many of these products, however, don’t undergo premarket approval (a review of safety and effectiveness by FDA experts before a product can be marketed). Majority of the time, the FDA’s enforcement efforts focus on products that are already on sale.
To help determine which products and Medical Supplies in California are FDA approved, here’s a guide to how the FDA regulates products and what their agency does (and doesn’t) approve.
The FDA doesn’t approve: companies, compounded drugs, tobacco products, cosmetics, medical foods, infant formula, dietary supplements, food label (including the Nutrition Facts panel), and structure-function claims on dietary supplements and other foods.
What the FDA does approve: new drugs and biologics, food additives in food for people, color additives used in FDA-regulated products, and animal drugs and food additives for use in food for animals.
To read the full guide, visit the FDA’s website, here.
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