Title 21

PART 570

Part 570 - Food Additives

PART 570 - FOOD ADDITIVES Authority:21 U.S.C. 321, 341, 342, 346a, 348, 371. Source:41 FR 38644, Sept. 10, 1976, unless otherwise noted.

• Authority: 21 U.S.C. 321, 341, 342, 346a, 348, 371.
• Source: 41 FR 38644, Sept. 10, 1976, unless otherwise noted.

21:6.0.1.1.21.1	SUBPART A	Subpart A - General Provisions
21:6.0.1.1.21.1.2.1	SECTION 570.3	570.3 Definitions.
21:6.0.1.1.21.1.2.2	SECTION 570.6	570.6 Opinion letters on food additive status.
21:6.0.1.1.21.1.2.3	SECTION 570.13	570.13 Indirect food additives resulting from packaging materials prior sanctioned for animal feed and pet food.
21:6.0.1.1.21.1.2.4	SECTION 570.14	570.14 Indirect food additives resulting from packaging materials for animal feed and pet food.
21:6.0.1.1.21.1.2.5	SECTION 570.15	570.15 Adoption of regulation on initiative of Commissioner.
21:6.0.1.1.21.1.2.6	SECTION 570.17	570.17 Exemption for investigational use and procedure for obtaining authorization to market edible products from experimental animals.
21:6.0.1.1.21.1.2.7	SECTION 570.18	570.18 Tolerances for related food additives.
21:6.0.1.1.21.1.2.8	SECTION 570.19	570.19 Pesticide chemicals in processed foods.
21:6.0.1.1.21.2	SUBPART B	Subpart B - Food Additive Safety
21:6.0.1.1.21.2.2.1	SECTION 570.20	570.20 General principles for evaluating the safety of food additives.
21:6.0.1.1.21.2.2.2	SECTION 570.30	570.30 Eligibility for classification as generally recognized as safe (GRAS).
21:6.0.1.1.21.2.2.3	SECTION 570.35	570.35 Affirmation of generally recognized as safe (GRAS) status.
21:6.0.1.1.21.2.2.4	SECTION 570.38	570.38 Determination of food additive status.
21:6.0.1.1.21.3	SUBPART C	Subparts C-D [Reserved]
21:6.0.1.1.21.4	SUBPART E	Subpart E - Generally Recognized as Safe (GRAS) Notice
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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