HR 4306 119th Congress
Food Chemical Reassessment Act of 2025
To amend the Federal Food, Drug, and Cosmetic Act to require the Office of Food Chemical Safety, Dietary Supplements, and Innovation to conduct food chemical safety reassessments, and for other purposes.
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Introduction Congress.gov
Introduced
Introduced in the House.
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Referred to the House Committee on Energy and Commerce.
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Introduced in House
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Introduced in House
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Introduced in House
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| Date and time | Record | Official detail | Source |
|---|---|---|---|
| IntroductionIntroduced | Introduced in the House. | Congress.gov | |
| Official actionReferred to the House Committee on Energy and Commerce. | No additional detail supplied.IntroReferral · House floor actions · Code H11100 | Congress.gov | |
| Official actionIntroduced in House | No additional detail supplied.IntroReferral · Library of Congress · Code Intro-H | Congress.gov | |
| Official actionIntroduced in House | No additional detail supplied.IntroReferral · Library of Congress · Code 1000 | Congress.gov | |
| Text versionIntroduced in House | A dated text-version record is available. | Congress.gov |
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Congressional Research Service
CRS summary
Food Chemical Reassessment Act of 2025This bill requires the Food and Drug Administration (FDA) to regularly reassess the safety of certain substances used in food and food packaging.Specifically, the FDA must select at least 10 substances or classes of substances for reassessment at least every three years. The FDA must select from color additives, food additives, substances generally recognized as safe (GRAS) for use in food, and other specified classes of substances. The FDA must prioritize substances for reassessment by public health need. The bill specifies certain substances that the FDA may select as the first to be reassessed, including titanium dioxide, sodium nitrite, and certain food dyes.These reassessments must be conducted by the FDA’s Office of Food Chemical Safety, Dietary Supplements, and Innovation.The FDA must provide public notice of its determination for each reassessed substance. Generally, if the FDA has issued a regulation or other order approving the use of a substance in food or food packaging, it must amend or repeal that regulation or order if it determines on reassessment that the substance is not safe. Any determination with respect to a GRAS substance must be published on the FDA’s website, and a determination that a GRAS substance is safe must include conditions of safe use.Finally, the FDA must reestablish the Food Advisory Committee to provide advice on standards and processes for these reassessments.
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Text versions
- Introduced in HouseJul 10, 2025