U.S. flag An official website of the United States government

On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.

  1. Home
  2. Regulatory Information
  3. Search for FDA Guidance Documents
  4. CPG Sec 585.325 Corn on the Cob, Canned - Quantity of Contents Declaration
  1. Search for FDA Guidance Documents

COMPLIANCE POLICY GUIDE (CPG)

CPG Sec 585.325 Corn on the Cob, Canned - Quantity of Contents Declaration November 2005

Final
Issued by:
Guidance Issuing Office
Human Foods Program
Office of Inspections and Investigations

BACKGROUND:

In the past we have advised packers of canned corn on the cob that the quantity of contents declaration should be in terms of both net weight and count.

Upon the basis of information supplied by the National Canners Association, we have concluded that a net weight declaration on canned corn on the cob would not be meaningful to consumers since such declaration would include the weight of the inedible cobs and the packing medium which is customarily discarded. A drained weight declaration, which would include the weight of the inedible cobs, would not be meaningful, and might be misleading, since drained weight declarations usually indicate the quantity of edible food in packages.

POLICY:

In order to satisfy the requirement of 21 CFR 101.105(a), the quantity of contents declaration on canned corn on the cob should be in terms of count (number of ears). We will not object to a declaration in terms of net weight also, but this is not required. The can should, of course, be well filled to avoid deception.

Issued: 1/22/70

Revised: 8/20/73

Reissued: 10/1/80

Revised: 12/8/88, 8/2005

Updated: 11/29/05


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

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 comments should be identified with the title of the guidance.

Back to Top