summary
Introduced
06/21/2023
06/21/2023
In Committee
06/21/2023
06/21/2023
Crossed Over
Passed
Dead
01/03/2025
01/03/2025
Introduced Session
118th Congress
Bill Summary
A bill 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.
AI Summary
This bill, the Allergen Disclosure In Non-food Articles Act (ADINA Act), amends the Federal Food, Drug, and Cosmetic Act to require the label of a drug intended for human use to identify each ingredient that is, or is derived from, a major food allergen or a gluten-containing grain (such as wheat, barley, or rye). This labeling requirement will apply either on a date determined by the Secretary of Health and Human Services or two years after the bill's enactment, whichever is earlier. The purpose of this bill is to provide consumers with more information about the potential allergens in their medications.
Committee Categories
Health and Social Services
Sponsors (2)
Last Action
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (on 06/21/2023)
Bill Topics
Health
- ‐ Regulation of Drug Industry and Pharmacies
Official Document
bill text
bill summary
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bill summary
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bill summary
| Document Type | Source Location | Created |
|---|---|---|
| State Bill Page | https://www.congress.gov/bill/118th-congress/senate-bill/2079/all-info | 06/22/2023 |
| BillText | https://www.congress.gov/118/bills/s2079/BILLS-118s2079is.pdf | 07/18/2023 |
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