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Library / Laws / 119th Congress / House Bills / H.R. 3821

H.R. 3821

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.

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Introduced in House2025-06-061.6K⠃⠗⠋