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U.S. Department of Health and Human Services

About FDA

Percentage of food contact substance notification reviews completed during the month within 110 days of original or amended receipt

Dictionary: FDA has the primary legal responsibility for determining the safe use of food and color additives. Before a food additive is marketed that will have technical effect in food, there must first be a regulation issued by FDA that authorizes such use. Similarly, before a color additive is marketed for use in food, drugs, cosmetics, or in certain medical devices, FDA must issue an authorizing regulation. A company that seeks a regulation for a new use of a food or color additive must submit a petition to FDA with evidence that the substance is safe for the intended use. A substance for which the use is generally recognized by qualified experts as safe is exempt from premarket approval as a food additive. "GRAS" is an acronym for the phrase Generally Recognized As Safe. The GRAS notification program is a voluntary procedure that is operating under a proposed rule issued in 1997. FDA reviews the notice and responds to the notifier by letter. In general, FDA’s response has been in one of three categories: does not question the basis for the GRAS determination, concludes the notice does not provide a sufficient basis for a GRAS determination, or at the notifier’s request has ceased to evaluate the GRAS notice.

FDA also has responsibility for the regulation of components of food contact materials (food contact substances) under the same authority as for direct food additives. To market a new food contact substance or an existing substance for a new use, manufacturers must notify FDA 120 days prior to marketing the substance. Notifications must establish that the proposed use is safe in accordance with the same safety standard as direct food additives. In the event safety is not established, FDA may object to the notification to prevent marketing. In addition, FDA may ask for additional information based on our review or request that a notifier withdraw a deficient notification.

Increasing the efficiency of review of food and color additive petitions, GRAS notices, and notifications for food contact substances:

  • Increases consumer choices for safe packaging materials, food ingredients, and color additives;
  • Provides consumers and industry with additional tools to mitigate or prevent microbial contamination that may lead to food borne illness; and
  • Maximizes the use of FDA resources applied to food safety and public health protection.

Information is current as of December 31, 2013.

Fiscal Year - 2013

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TimeAnnual TargetPercentage
Oct 201270100
Nov 20127088
Dec 201270100
Jan 20137083
Feb 20127067
Mar 201370100
Apr 201370100
May 20137083
Jun 201370100
Jul 201370100
Aug 201370100
Sep 20137095

FY 2013 Overall: 95%

Number of food contact substance notification reviews completed during the month within 110 days of original or amended receipt

Fiscal Year - 2013
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TimeAnnual TargetNumber
Oct 2012N/A10
Nov 2012N/A7
Dec 2012N/A3
Jan 2013N/A10
Feb 2013N/A2
Mar 2013N/A12
Apr 2013N/A11
May 2013N/A5
Jun 2013N/A14
Jul 2013N/A8
Aug 2013N/A9
Sep 2013N/A36

FY 2013 Total: 127

Total number of food contact substance notification reviews completed during the month

Fiscal Year - 2013
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TimeAnnual TargetNumber
Oct 2012N/A10
Nov 2012N/A8
Dec 2012N/A3
Jan 2013N/A12
Feb 2013N/A3
Mar 2013N/A12
Apr 2013N/A11
May 2013N/A6
Jun 2013N/A14
Jul 2013N/A8
Aug 2013N/A9
Sep 2013N/A38

FY 2013 Total: 134

Median number of days to complete review during the month

Fiscal Year - 2013
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TimeAnnual TargetNumber
Oct 2012N/A91
Nov 2012N/A79
Dec 2012N/A94
Jan 2013N/A78
Feb 2013N/A109
Mar 2013N/A80
Apr 2013N/A61
May 2013N/A93
Jun 2013N/A66
Jul 2013N/A71
Aug 2013N/A87
Sep 2013N/A75

FY 2013 Total: 80

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.