TITLE 21--FOOD AND DRUGS 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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