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FEDERAL · 21 CFR

Part 570 — Food Additives

28 sections · Title 21: Food and Drugs

§ 570.3Definitions.
§ 570.6Opinion letters on food additive status.
§ 570.13Indirect food additives resulting from packaging materials prior sanctioned for animal feed and pet food.
§ 570.14Indirect food additives resulting from packaging materials for animal feed and pet food.
§ 570.15Adoption of regulation on initiative of Commissioner.
§ 570.17Exemption for investigational use and procedure for obtaining authorization to market edible products from experimental animals.
§ 570.18Tolerances for related food additives.
§ 570.19Pesticide chemicals in processed foods.
§ 570.20General principles for evaluating the safety of food additives.
§ 570.30Eligibility for classification as generally recognized as safe (GRAS).
§ 570.35Affirmation of generally recognized as safe (GRAS) status.
§ 570.38Determination of food additive status.
§ 570.203Definitions.
§ 570.205Opportunity to submit a GRAS notice.
§ 570.210How to send your GRAS notice to FDA.
§ 570.215Incorporation into a GRAS notice.
§ 570.220General requirements applicable to a GRAS notice.
§ 570.225Part 1 of a GRAS notice: Signed statements and certification.
§ 570.230Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
§ 570.235Part 3 of a GRAS notice: Target animal and human exposures.
§ 570.240Part 4 of a GRAS notice: Self-limiting levels of use.
§ 570.245Part 5 of a GRAS notice: Experience based on common use in food before 1958.
§ 570.250Part 6 of a GRAS notice: Narrative.
§ 570.255Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
§ 570.260Steps you may take before FDA responds to your GRAS notice.
§ 570.265What FDA will do with a GRAS notice.
§ 570.275Public disclosure of a GRAS notice.
§ 570.280Submission of a supplement.