Library / Laws / 116th Congress / Senate Bills / S. 3021
S. 3021
To amend the Federal Food, Drug, and Cosmetic Act to require the label of a drug that is intended for human use and contains an ingredient that is derived directly or indirectly from a gluten-containing grain to identify each such ingredient, and for other purposes.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in Senate | 2019-12-11 | 1.5K | ⠃⠗⠋ |