Referred to the House Committee on Energy and Commerce.
Summary
The bill amends the Federal Food, Drug, and Cosmetic Act to make manufacturers, packers, distributors, or their U.S. agents submit detailed information about each dietary supplement to the FDA. A unique listing number is then assigned and must appear on the product label. This is intended to give consumers and regulators clearer information about supplement contents and claims.
AI-generated summary — may be incomplete or inaccurate. Verify against the official bill text.
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