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Food Safety: New Rules for Ingredients in Food Products

This act introduces new rules for ingredients added to food that are generally recognized as safe. Companies will need to notify the Food and Drug Administration (FDA) before using these ingredients, and the FDA will review them more thoroughly. The goal is to enhance the safety of the food we buy in stores by better controlling what goes into our meals.
Key points
Companies must notify the FDA of new 'generally recognized as safe' (GRAS) ingredients before using them in food.
The FDA will systematically reassess the safety of at least 10 substances or classes every three years, including those already deemed safe.
The FDA can object to or revoke approval for an ingredient if safety concerns arise.
Information on notified ingredients and FDA decisions will be publicly available, with opportunities for public comment.
Fees will be introduced for companies to cover the costs of ingredient notifications and reassessments by the FDA.
article Official text account_balance Process page
Introduced
Citizen Poll
No votes cast
Additional Information
Print number: 119_HR_4958
Sponsor: Rep. Pallone, Frank [D-NJ-6]
Process start date: 2025-08-12
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Summarized by: gemini-2.5-flash
Source data: api.congress.gov
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OFFICIAL LEGAL TITLE

GRAS Act

FREQUENTLY ASKED QUESTIONS

What is the official ID of this bill?

The official print number for this legislation is 119_HR_4958.

Which chamber initiated this legislation?

This legislation was initiated in the House of Representatives.

When did the legislative process begin?

The process officially started on 2025-08-12.

What are the main provisions?

Key points include:

  • Companies must notify the FDA of new 'generally recognized as safe' (GRAS) ingredients before using them in food.
  • The FDA will systematically reassess the safety of at least 10 substances or classes every three years, including those already deemed safe.
  • The FDA can object to or revoke approval for an ingredient if safety concerns arise.
  • Information on notified ingredients and FDA decisions will be publicly available, with opportunities for public comment.
  • Fees will be introduced for companies to cover the costs of ingredient notifications and reassessments by the FDA.
What is the specific legal status?

The current status is Introduced.

Where can I read the full text of this legislation?

The full official text is available at: View full text

Who is the primary sponsor?

The primary sponsor is Rep. Pallone, Frank [D-NJ-6].

What is the latest detailed status?

The latest detailed status is: Referred to the House Committee on Energy and Commerce.

Is this summary verified?

Yes. This content was analyzed by AI and verified by the Lustra Judge System on 2025-12-23.

CATEGORIES

Health