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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter E - Animal Drugs, Feeds, and Related Products |
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Part 570 - Food Additives |
| 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 - XXX |
| 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. |