Generally Recognized as Safe (GRAS) Notice | Midpage

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Code of Federal Regulations

Subpart E

Generally Recognized as Safe (GRAS) Notice

170.203Definitions.170.205Opportunity to submit a GRAS notice.170.210How to send your GRAS notice to FDA.170.215Incorporation into a GRAS notice.170.220General requirements applicable to a GRAS notice.170.225Part 1 of a GRAS notice: Signed statements and certification.170.230Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.170.235Part 3 of a GRAS notice: Dietary exposure.170.240Part 4 of a GRAS notice: Self-limiting levels of use.170.245Part 5 of a GRAS notice: Experience based on common use in food before 1958.170.250Part 6 of a GRAS notice: Narrative.170.255Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.170.260Steps you may take before FDA responds to your GRAS notice.170.265What FDA will do with a GRAS notice.170.270Procedures that apply when the intended conditions of use of a notified substance include use in a product or products subject to regulation by the Food Safety and Inspection Service (FSIS) of the United States Department of Agriculture.170.275Public disclosure of a GRAS notice.170.280Submission of a supplement.170.285Disposition of pending GRAS affirmation petitions.