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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 B - Food for Human Consumption |
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Part 170 - Food Additives |
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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. |