Title 21

PART 570 SUBPART E

Subpart E - Generally Recognized as Safe (GRAS) Notice Source:81 FR 55052, Aug. 17, 2016, unless otherwise noted.

21:6.0.1.1.21.4.2.1SECTION 570.203
   570.203 Definitions.
21:6.0.1.1.21.4.2.2SECTION 570.205
   570.205 Opportunity to submit a GRAS notice.
21:6.0.1.1.21.4.2.3SECTION 570.210
   570.210 How to send your GRAS notice to FDA.
21:6.0.1.1.21.4.2.4SECTION 570.215
   570.215 Incorporation into a GRAS notice.
21:6.0.1.1.21.4.2.5SECTION 570.220
   570.220 General requirements applicable to a GRAS notice.
21:6.0.1.1.21.4.2.6SECTION 570.225
   570.225 Part 1 of a GRAS notice: Signed statements and certification.
21:6.0.1.1.21.4.2.7SECTION 570.230
   570.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
21:6.0.1.1.21.4.2.8SECTION 570.235
   570.235 Part 3 of a GRAS notice: Target animal and human exposures.
21:6.0.1.1.21.4.2.9SECTION 570.240
   570.240 Part 4 of a GRAS notice: Self-limiting levels of use.
21:6.0.1.1.21.4.2.10SECTION 570.245
   570.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958.
21:6.0.1.1.21.4.2.11SECTION 570.250
   570.250 Part 6 of a GRAS notice: Narrative.
21:6.0.1.1.21.4.2.12SECTION 570.255
   570.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
21:6.0.1.1.21.4.2.13SECTION 570.260
   570.260 Steps you may take before FDA responds to your GRAS notice.
21:6.0.1.1.21.4.2.14SECTION 570.265
   570.265 What FDA will do with a GRAS notice.
21:6.0.1.1.21.4.2.15SECTION 570.275
   570.275 Public disclosure of a GRAS notice.
21:6.0.1.1.21.4.2.16SECTION 570.280
   570.280 Submission of a supplement.