Dietary Supplement Listing Act of 2026 requires manufacturers to list dietary supplements with the FDA.
The Dietary Supplement Listing Act of 2026 amends the Federal Food, Drug, and Cosmetic Act to require manufacturers, packers, or distributors of dietary supplements to list their products with the Food and Drug Administration (FDA). The responsible person must submit detailed information about each dietary supplement, including ingredients, serving sizes, and directions for use. The FDA will assign a unique dietary supplement product listing number and maintain a publicly searchable electronic database of listed supplements.
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- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
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