ADINA Act
The ADINA Act requires drug manufacturers to clearly label human-use drugs containing major food allergens (like peanuts or shellfish) or ingredients derived from gluten-containing grains (wheat, barley, rye). This directly affects drug companies producing such medications by mandating specific allergen disclosure on product labels. The key provision adds new labeling requirements to the Federal Food, Drug, and Cosmetic Act, forcing manufacturers to state both the presence of the allergen and its source. The rule takes effect within two years of the bill's enactment. This policy change ensures consumers with allergies can identify potential risks in prescription and over-the-counter drugs.
Bill status
in committee
1 of 4 stages cleared
Introduction
Jun 2023
Committee Review
Floor Vote
President
Introduced Jun 21, 2023
Last action Jun 21, 2023
Floor votes
How they voted
No floor votes recorded yet.
Full legislative history
Actions timeline
Total actions
2
Key actions
0
Committee
1
Jun 21, 2023
Committee
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
upper
Jun 21, 2023
Introduced
Introduced in Senate
upper
1 primary · 1 co-sponsor
Sponsors
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