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.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in House | 2025-06-06 | 1.6K | ⠃⠗⠋ |