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.
No official summary available for this bill.
Introduced in House
Introduced in House
Sponsor introductory remarks on measure. (CR H2516)
Referred to the House Committee on Energy and Commerce.
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