Subpart E—Generally Recognized as Safe (GRAS) Notice
Sections
Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.
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170.203
§ 170.203 Definitions. -
170.205
§ 170.205 Opportunity to submit a GRAS notice. -
170.210
§ 170.210 How to send your GRAS notice to FDA. -
170.215
§ 170.215 Incorporation into a GRAS notice. -
170.220
§ 170.220 General requirements applicable to a GRAS notice. -
170.225
§ 170.225 Part 1 of a GRAS notice: Signed statements and certification. -
170.230
§ 170.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect. -
170.235
§ 170.235 Part 3 of a GRAS notice: Dietary exposure. -
170.240
§ 170.240 Part 4 of a GRAS notice: Self-limiting levels of use. -
170.245
§ 170.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958. -
170.250
§ 170.250 Part 6 of a GRAS notice: Narrative. -
170.255
§ 170.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice. -
170.260
§ 170.260 Steps you may take before FDA responds to your GRAS notice. -
170.265
§ 170.265 What FDA will do with a GRAS notice. -
170.270
§ 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
§ 170.275 Public disclosure of a GRAS notice. -
170.280
§ 170.280 Submission of a supplement. -
170.285
§ 170.285 Disposition of pending GRAS affirmation petitions.