 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter B - Food for Human Consumption |
|
|
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 |
| § 170.45 - Fluorine-containing compounds. |
| § 170.50 - Glycine (aminoacetic acid) in food for human consumption. |
| § 170.60 - Nitrites and/or nitrates in curing premixes. |
| 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. |
| § 170.275 - Public disclosure of a GRAS notice. |
| § 170.280 - Submission of a supplement. |
| § 170.285 - Disposition of pending GRAS affirmation petitions. |