21 CFR Part 570
PART 570—FOOD ADDITIVES
- PART 570—FOOD ADDITIVES
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter E—Animal Drugs, Feeds, and Related Products
- Subpart A—General Provisions
- § 570.3 Definitions.
- § 570.6 Opinion letters on food additive status.
- § 570.13 Indirect food additives resulting from packaging materials prior sanctioned for animal feed and pet food.
- § 570.14 Indirect food additives resulting from packaging materials for animal feed and pet food.
- § 570.15 Adoption of regulation on initiative of Commissioner.
- § 570.17 Exemption for investigational use and procedure for obtaining authorization to market edible products from experimental animals.
- § 570.18 Tolerances for related food additives.
- § 570.19 Pesticide chemicals in processed foods.
- Subpart B—Food Additive Safety
- § 570.20 General principles for evaluating the safety of food additives.
- § 570.30 Eligibility for classification as generally recognized as safe (GRAS).
- § 570.35 Affirmation of generally recognized as safe (GRAS) status.
- § 570.38 Determination of food additive status.
- Subparts C-D [Reserved]
- Subpart E—Generally Recognized as Safe (GRAS) Notice
- § 570.203 Definitions.
- § 570.205 Opportunity to submit a GRAS notice.
- § 570.210 How to send your GRAS notice to FDA.
- § 570.215 Incorporation into a GRAS notice.
- § 570.220 General requirements applicable to a GRAS notice.
- § 570.225 Part 1 of a GRAS notice: Signed statements and certification.
- § 570.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- § 570.235 Part 3 of a GRAS notice: Target animal and human exposures.
- § 570.240 Part 4 of a GRAS notice: Self-limiting levels of use.
- § 570.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- § 570.250 Part 6 of a GRAS notice: Narrative.
- § 570.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- § 570.260 Steps you may take before FDA responds to your GRAS notice.
- § 570.265 What FDA will do with a GRAS notice.
- § 570.275 Public disclosure of a GRAS notice.
- § 570.280 Submission of a supplement.
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