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ADINA Act
To amend the Federal Food, Drug, and Cosmetic Act to require the label of a drug intended for human use to identify each ingredient in such drug that is, or is derived directly or indirectly from, a major food allergen or a gluten-containing grain, and for other purposes.
- Introduced
- Committee
- Passed House
- Passed Senate
- To President
- Became law
Summary
The Congressional Research Service has not published a summary of this bill yet.
Actions
- Jun 6, 2025 Referred to the House Committee on Energy and Commerce.
- Jun 6, 2025 Sponsor introductory remarks on measure. (CR H2516)
- Jun 6, 2025 Introduced in House
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