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The expiration date of pharmaceuticals specifies the date the manufacturer guarantees the full potency and safety of a drug. Most medications continue to be effective and safe for a time after the expiration date. A rare exception is a case of renal tubular acidosis purportedly caused by expired tetracycline. [7]
Manufacturers of dietary supplements are permitted to make specific claims of health benefits, referred to as "structure or function claims" on the labels of these products. [6] They may not claim to treat, diagnose, cure, or prevent disease and must include a disclaimer on the label. [ 41 ]
Senator Orrin Hatch of Utah introduced the Health Freedom Act of 1992 which would have blocked the FDA from using health claims as a reason to regulate dietary supplements as drugs. The senator said he "entered the controversy after hearing from constituents in his home state, including both consumers and makers of dietary supplements".
The FDA can only ban a supplement if the FDA finds proof that the supplement is dangerous. This means that unsafe or ineffective supplements can be sold freely, while the FDA has only a limited capacity to monitor adverse reactions from supplements. [19] [20] David Kessler, commissioner of the FDA when DSHEA was approved, has stated that
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A new rule from the Food and Drug Administration (FDA) will update what it means for food to be labeled “healthy” for the first time in 30 years, a move that aligns with current nutrition ...
The Center for Food Safety and Applied Nutrition (CFSAN (/ ˈ s ɪ f ˌ s æ n / SIF-san)) is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements, and cosmetics, as opposed to drugs, biologics, medical devices, and radiological products, which also fall under the purview of the FDA.
The FDA doesn’t recommend using expired COVID at-home tests that do not have an expiration date extension. “COVID-19 tests and the parts they are made of may degrade, or break down, over time.