FDA Issues Draft Guidance on Proper Labeling of Honey Products
The U.S. Food and Drug Administration (FDA) yesterday issued draft guidance for industry entitled “Guidance for Industry: Proper Labeling of Honey and Honey Products.”
As noted in the Federal Register notice published today, FDA issued the draft guidance to help members of the food industry ensure they are properly labeling honey and honey products, and to remind them that honey and honey products must not be misbranded or adulterated under the provisions of the Federal Food, Drug, and Cosmetic Act.