Part 170 — Food Additives
Subpart A — General Provisions
- § 170.3— Definitions.
- § 170.6— Opinion letters on food additive status.
- § 170.10— Food additives in standardized foods.
- § 170.15— Adoption of regulation on initiative of Commissioner.
- § 170.17— Exemption for investigational use and procedure for obtaining authorization to market edible products from experimental animals.
- § 170.18— Tolerances for related food additives.
- § 170.19— Pesticide chemicals in processed foods.
Subpart B — Food Additive Safety
- § 170.20— General principles for evaluating the safety of food additives.
- § 170.22— Safety factors to be considered.
- § 170.30— Eligibility for classification as generally recognized as safe (GRAS).
- § 170.35— Affirmation of generally recognized as safe (GRAS) status.
- § 170.38— Determination of food additive status.
- § 170.39— Threshold of regulation for substances used in food-contact articles.
Subpart C — Specific Administrative Rulings and Decisions
Subpart D — Premarket Notifications
- § 170.100— Submission of a premarket notification for a food contact substance (FCN) to the Food and Drug Administration (FDA).
- § 170.101— Information in a premarket notification for a food contact substance (FCN).
- § 170.102— Confidentiality of information related to premarket notification for a food contact substance (FCN).
- § 170.103— Withdrawal without prejudice of a premarket notification for a food contact substance (FCN).
- § 170.104— Action on a premarket notification for a food contact substance (FCN).
- § 170.105— The Food and Drug Administration's (FDA's) determination that a premarket notification for a food contact substance (FCN) is no longer effective.
- § 170.106— Notification for a food contact substance formulation (NFCSF).
Subpart E — Generally Recognized as Safe (GRAS) Notice
- § 170.203— Definitions.
- § 170.205— Opportunity to submit a GRAS notice.
- § 170.210— How to send your GRAS notice to FDA.
- § 170.215— Incorporation into a GRAS notice.
- § 170.220— General requirements applicable to a GRAS notice.
- § 170.225— Part 1 of a GRAS notice: Signed statements and certification.
- § 170.230— Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- § 170.235— Part 3 of a GRAS notice: Dietary exposure.
- § 170.240— Part 4 of a GRAS notice: Self-limiting levels of use.
- § 170.245— Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- § 170.250— Part 6 of a GRAS notice: Narrative.
- § 170.255— Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- § 170.260— Steps you may take before FDA responds to your GRAS notice.
- § 170.265— What FDA will do with a GRAS notice.
- § 170.270— Procedures 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.
- § 170.275— Public disclosure of a GRAS notice.
- § 170.280— Submission of a supplement.
- § 170.285— Disposition of pending GRAS affirmation petitions.