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e-CFR data is current as of January 19, 2021

Title 21 → Chapter I → Subchapter E → Part 570

TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS

PART 570—FOOD ADDITIVES

rule

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.
rule

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.
rule

Subparts C-D [Reserved]

rule

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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