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Regulations last checked for updates: Sep 01, 2025
Title 21 - Food and Drugs last revised: Aug 22, 2025
All Titles
Title 21
Chapter I
Part 170
Subpart E - Subpart E—Generally Recognized as Safe (GRAS) Notice
§ 170.203 - Definitions.
§ 170.205 - Opportunity to submit a GRAS notice.
§ 170.210 - How to send your GRAS notice to FDA.
§ 170.215 - Incorporation into a GRAS notice.
§ 170.220 - General requirements applicable to a GRAS notice.
§ 170.225 - Part 1 of a GRAS notice: Signed statements and certification.
§ 170.230 - Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
§ 170.235 -
§ 170.240 - Part 4 of a GRAS notice: Self-limiting levels of use.
§ 170.245 - Part 5 of a GRAS notice: Experience based on common use in food before 1958.
§ 170.250 - Part 6 of a GRAS notice: Narrative.
§ 170.255 - Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
§ 170.260 - Steps you may take before FDA responds to your GRAS notice.
§ 170.265 - What FDA will do with a GRAS notice.
§ 170.270 - Procedures 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.
§ 170.275 - Public disclosure of a GRAS notice.
§ 170.280 - Submission of a supplement.
§ 170.285 - Disposition of pending GRAS affirmation petitions.
authority:
21 U.S.C. 321
,
341
,
342
,
346a
,
348
,
371
source:
42 FR 14483, Mar. 15, 1977, unless otherwise noted.
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