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 U.S.C. 321, 341, 342, 346a, 348, 371.
• Source: 41 FR 38644, Sept. 10, 1976, unless otherwise noted.

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

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