Subpart E—Generally Recognized as Safe (GRAS) Notice

1. CFR
2. ›
3. Title 21
4. ›
5. Chapter I
6. ›
7. Part 170
8. ›
9. Subpart E

Sections

Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.

• 170.203
  § 170.203 Definitions.
• 170.205
  § 170.205 Opportunity to submit a GRAS notice.
• 170.210
  § 170.210 How to send your GRAS notice to FDA.
• 170.215
  § 170.215 Incorporation into a GRAS notice.
• 170.220
  § 170.220 General requirements applicable to a GRAS notice.
• 170.225
  § 170.225 Part 1 of a GRAS notice: Signed statements and certification.
• 170.230
  § 170.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
• 170.235
  § 170.235 Part 3 of a GRAS notice: Dietary exposure.
• 170.240
  § 170.240 Part 4 of a GRAS notice: Self-limiting levels of use.
• 170.245
  § 170.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958.
• 170.250
  § 170.250 Part 6 of a GRAS notice: Narrative.
• 170.255
  § 170.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
• 170.260
  § 170.260 Steps you may take before FDA responds to your GRAS notice.
• 170.265
  § 170.265 What FDA will do with a GRAS notice.
• 170.270
  § 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
  § 170.275 Public disclosure of a GRAS notice.
• 170.280
  § 170.280 Submission of a supplement.
• 170.285
  § 170.285 Disposition of pending GRAS affirmation petitions.