Generally Recognized as Safe (GRAS) Notice

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Food for Human Consumption
  6. Food Additives
  7. Generally Recognized as Safe (GRAS) Notice

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Section
170.203

Definitions.

Section
170.205

Opportunity to submit a GRAS notice.

Section
170.210

How to send your GRAS notice to FDA.

Section
170.215

Incorporation into a GRAS notice.

Section
170.220

General requirements applicable to a GRAS notice.

Section
170.225

Part 1 of a GRAS notice: Signed statements and certification.

Section
170.230

Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.

Section
170.235

Part 3 of a GRAS notice: Dietary exposure.

Section
170.240

Part 4 of a GRAS notice: Self-limiting levels of use.

Section
170.245

Part 5 of a GRAS notice: Experience based on common use in food before 1958.

Section
170.250

Part 6 of a GRAS notice: Narrative.

Section
170.255

Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.

Section
170.260

Steps you may take before FDA responds to your GRAS notice.

Section
170.265

What FDA will do with a GRAS notice.

Section
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.

Section
170.275

Public disclosure of a GRAS notice.

Section
170.280

Submission of a supplement.

Section
170.285

Disposition of pending GRAS affirmation petitions.