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FDA Defines “Gluten-Free”

On Friday, Aug. 2, 2013, the U.S. Food and Drug Administration (FDA) published a new regulation defining the term “gluten-free” for voluntary food labeling. In order to be labeled as “gluten-free,” “no gluten,” “free of gluten” or “without gluten,” the food must contain less than 20 parts per million of gluten.

The term “gluten” refers to proteins that occur naturally in wheat, rye, barley and cross-bred hybrids of these grains. For individuals with the autoimmune digestive condition celiac disease, the gluten in food triggers the production of antibodies that attack and damage the lining of the small intestine and limits their ability to absorb nutrients. Celiac disease can be effectively managed only by eating a gluten free diet.

FDA deputy commissioner, Michael R. Taylor, stated: “We encourage the food industry to come into compliance with the new definition as soon as possible and help make it as easy as possible for people with celiac disease to identify foods that meet the federal definition of ‘gluten-free.’”

Food manufactures will have one year after the rule is published to bring their labels into compliance with this new requirement.

For more information, please contact the Barnes & Thornburg LLP attorney with whom you work or Joan Long (312-214-4576) of the firm’s Advertising and Marketing group.

© 2013 Barnes & Thornburg LLP. All Rights Reserved. This page, and all information on it, is proprietary and the property of Barnes & Thornburg LLP. It may not be reproduced, in any form, without the express written consent of Barnes & Thornburg LLP.

This Barnes & Thornburg LLP publication should not be construed as legal advice or legal opinion on any specific facts or circumstances. The contents are intended for general informational purposes only, and you are urged to consult your own lawyer on any specific legal questions you may have concerning your situation.



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