The ADINA Act mandates drug labels to disclose major food allergens and gluten-containing grains.
The ADINA Act amends the Federal Food, Drug, and Cosmetic Act to require drug labels to identify ingredients that are major food allergens or derived from gluten-containing grains. This applies to drugs intended for human use, with compliance required by a specified date. The act aims to ensure consumers are informed about potential allergens in their medications.
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- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
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