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ADINA Act
6/30/2025, 1:09 PM
Summary of Bill HR 3821
The bill, H.R. 3821 of the 119th Congress, seeks to amend the Federal Food, Drug, and Cosmetic Act to mandate that drug labels intended for human use must specify each ingredient that is directly or indirectly derived from a major food allergen or a gluten-containing grain.
Read the Full Bill
Current Status of Bill HR 3821
Bill HR 3821 is currently in the status of Bill Introduced since June 6, 2025. Bill HR 3821 was introduced during Congress 119 and was introduced to the House on June 6, 2025. Bill HR 3821's most recent activity was Referred to the House Committee on Energy and Commerce. as of June 6, 2025
Bipartisan Support of Bill HR 3821
Total Number of Sponsors
5Democrat Sponsors
5Republican Sponsors
0Unaffiliated Sponsors
0Total Number of Cosponsors
11Democrat Cosponsors
3Republican Cosponsors
8Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill HR 3821
Primary Policy Focus
HealthAlternate Title(s) of Bill HR 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.
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.
Comments

Raul Grant
557
8 months ago
This bill bad for us.
Sponsors and Cosponsors of HR 3821
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