Inventory of Petitions Received under 21 U.S.C. 343(w)(6) for Exemptions from Food Allergen Labeling

The Federal Food, Drug, and Cosmetic Act (the Act) governs the labeling of all foods (except meat products, poultry products, and certain egg products, which are regulated by the U.S. Department of Agriculture.) The Food Allergen Labeling and Consumer Protection Act (FALCPA) (Pub L. 108-282) amends the Act's labeling requirements for food ingredients. FALCPA's requirements apply to packaged foods, including conventional foods, dietary supplements, infant formula, and medical foods, all of which are "food" within the Act's definition, 21 U.S.C. 321(f). FALCPA requires that an ingredient (including a flavor, color, or incidental additive) that is a "major food allergen," as defined by 21 U.S.C. 321(qq), be more explicitly identified on the food label. Under FALCPA, a "major food allergen" is one of eight foods or food groups (milk, eggs, fish, Crustacean shellfish, tree nuts, wheat, peanuts, and soybeans) or an ingredient that contains protein derived from one of the eight. 21 U.S.C. 321(qq). "Major food allergen" does not include a highly refined oil derived from one of the eight foods or food groups or any ingredient derived from such an oil, as well as any ingredient exempt under a statutory exemption process.

FALCPA establishes a process under 21 U.S.C. 343(w)(6) by which any person may file a petition that provides scientific evidence (including the analytical method used to produce the evidence) that demonstrates that an ingredient, as derived by the method specified in the petition, does not cause an allergenic response that poses a risk to human health. FDA has 180 days to approve or deny the petition. Absent an approval or denial within 180 days, the petition is deemed denied, unless FDA and the petitioner mutually agreed on an extension of time for FDA's response

FDA is required to post to a public site petitions received under 21 U.S.C. 343(w)(6) within 14 days of receipt. The petitions received by FDA are listed below and are on display at FDA's Division of Dockets Management, 5630 Fishers Lane, Room 1061 (HFA-305), Rockville, MD, 20852.

FALP No.Docket No.Date ReceivedPetitioner /
Ingredient Manufacturer
DescriptionMajor Food AllergenAgency Response
004FDA-2016-FL-1494October 29, 2015Archer Daniels Midland CompanySoy lecithin used a release agent.Soy
003FDA-2007-FL-0471June 14, 2007The Solae CompanySoy lecithin used as processing aidSoy
0022006FL-0384September 11, 2006The Solae CompanySoy lecithin used as processing aidSoyWithdrawn by petitioner, April 25, 2007
001FDA-2006-FL-0532June 5, 2006International Media and Cultures, Inc.Starter Growth MediaSoyObjection letter dated November 30, 2006


Page Last Updated: 07/16/2018
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English