U.S. flag An official website of the United States government
  1. Home
  2. Regulatory Information
  3. Search for FDA Guidance Documents
  4. CPG Sec 555.250 DRAFT: Major Food Allergen Labeling and Cross-contact
  1. Search for FDA Guidance Documents

COMPLIANCE POLICY GUIDE (CPG)

CPG Sec 555.250 DRAFT: Major Food Allergen Labeling and Cross-contact May 2023

Draft

Not for implementation. Contains non-binding recommendations.

This guidance is being distributed for comment purposes only.

Submit Comments by

Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the FDA considers your comment on a draft guidance before it begins work on the final version of the guidance, submit either online or written comments on the draft guidance before the close date.

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2023-D-1103


Docket Number:
FDA-2023-D-1103
Issued by:
Guidance Issuing Office
Center for Food Safety and Applied Nutrition, Office of Compliance

May 16, 2023 

This draft guidance, when finalized, will replace existing guidance, CPG Sec 555.250 Statement of Policy for Labeling and Preventing Cross-contact of Common Food Allergens, for FDA staff on FDA’s enforcement policy regarding major food allergen labeling and cross-contact.

The purpose of this compliance policy guide (CPG) is to provide guidance for FDA staff on FDA’s enforcement policy regarding major food allergen labeling and cross-contact. See section II.B for more information about major food allergens, which are defined in section 201(qq) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 321(qq)).

In general, FDA’s guidance documents do not establish legally enforceable responsibilities. Instead, guidances describe FDA’s current thinking on a topic and should be viewed only as recommendations, unless specific regulatory or statutory requirements are cited. The use of the word should in FDA guidances means that something is suggested or recommended, but not required.

Download the Draft CPG

Back to Top