Subpart E—Generally Recognized as Safe (GRAS) Notice

1. CFR
2. ›
3. Title 21
4. ›
5. Chapter I
6. ›
7. Part 570
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.

• 570.203
  § 570.203 Definitions.
• 570.205
  § 570.205 Opportunity to submit a GRAS notice.
• 570.210
  § 570.210 How to send your GRAS notice to FDA.
• 570.215
  § 570.215 Incorporation into a GRAS notice.
• 570.220
  § 570.220 General requirements applicable to a GRAS notice.
• 570.225
  § 570.225 Part 1 of a GRAS notice: Signed statements and certification.
• 570.230
  § 570.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
• 570.235
  § 570.235 Part 3 of a GRAS notice: Target animal and human exposures.
• 570.240
  § 570.240 Part 4 of a GRAS notice: Self-limiting levels of use.
• 570.245
  § 570.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958.
• 570.250
  § 570.250 Part 6 of a GRAS notice: Narrative.
• 570.255
  § 570.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
• 570.260
  § 570.260 Steps you may take before FDA responds to your GRAS notice.
• 570.265
  § 570.265 What FDA will do with a GRAS notice.
• 570.275
  § 570.275 Public disclosure of a GRAS notice.
• 570.280
  § 570.280 Submission of a supplement.