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FEDERAL · 21 CFR

Part 170 — Food Additives

41 sections · Title 21: Food and Drugs

§ 170.3Definitions.
§ 170.6Opinion letters on food additive status.
§ 170.10Food additives in standardized foods.
§ 170.15Adoption of regulation on initiative of Commissioner.
§ 170.17Exemption for investigational use and procedure for obtaining authorization to market edible products from experimental animals.
§ 170.18Tolerances for related food additives.
§ 170.19Pesticide chemicals in processed foods.
§ 170.20General principles for evaluating the safety of food additives.
§ 170.22Safety factors to be considered.
§ 170.30Eligibility for classification as generally recognized as safe (GRAS).
§ 170.35Affirmation of generally recognized as safe (GRAS) status.
§ 170.38Determination of food additive status.
§ 170.39Threshold of regulation for substances used in food-contact articles.
§ 170.45Fluorine-containing compounds.
§ 170.50Glycine (aminoacetic acid) in food for human consumption.
§ 170.60Nitrites and/or nitrates in curing premixes.
§ 170.100Submission of a premarket notification for a food contact substance (FCN) to the Food and Drug Administration (FDA).
§ 170.101Information in a premarket notification for a food contact substance (FCN).
§ 170.102Confidentiality of information related to premarket notification for a food contact substance (FCN).
§ 170.103Withdrawal without prejudice of a premarket notification for a food contact substance (FCN).
§ 170.104Action on a premarket notification for a food contact substance (FCN).
§ 170.105The Food and Drug Administration's (FDA's) determination that a premarket notification for a food contact substance (FCN) is no longer effective.
§ 170.106Notification for a food contact substance formulation (NFCSF).
§ 170.203Definitions.
§ 170.205Opportunity to submit a GRAS notice.
§ 170.210How to send your GRAS notice to FDA.
§ 170.215Incorporation into a GRAS notice.
§ 170.220General requirements applicable to a GRAS notice.
§ 170.225Part 1 of a GRAS notice: Signed statements and certification.
§ 170.230Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
§ 170.235Part 3 of a GRAS notice: Dietary exposure.
§ 170.240Part 4 of a GRAS notice: Self-limiting levels of use.
§ 170.245Part 5 of a GRAS notice: Experience based on common use in food before 1958.
§ 170.250Part 6 of a GRAS notice: Narrative.
§ 170.255Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
§ 170.260Steps you may take before FDA responds to your GRAS notice.
§ 170.265What FDA will do with a GRAS notice.
§ 170.270Procedures that apply when the intended conditions of use of a notified substance include use in a product or products subject to regulation by the Food Safety and Inspection Service (FSIS) of the United States Department of Agriculture.
§ 170.275Public disclosure of a GRAS notice.
§ 170.280Submission of a supplement.
§ 170.285Disposition of pending GRAS affirmation petitions.