The Food and Drug Administration will allow the “safe use” of chromium propionate as a source of chromium in broiler chicken feed, in response to a food additive petition filed by Kemin Industries, FDA said (here). The agency's final rule takes effect June 3, and objections and hearing requests are due July 2.
The Food and Drug Administration Philadelphia District Office, with co-sponsors the North Central Association of Food and Drug Officials and the Association of Food and Drug Officials, is holding a conference June 25-29 in Pittsburgh to provide industry members with information about FDA drug and device regulations, FDA said (here).
On May 31 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On May 27 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 12 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration issued its weekly Enforcement Report for May 25 that lists the status of recalls and field corrections for food, drugs, biologics, and devices (here). The report covers both domestic and foreign firms.
On May 25 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On May 24 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
Sweeteners derived from sugar cane should be listed on ingredient statements as sugar, said the Food and Drug Administration in a guidance document released on May 25 (here). Representing such ingredients as “evaporated cane juice” is considered by FDA to be “false and misleading,” said the agency. Sweeteners derived from sugar cane are not relevant to the percentage juice declaration on beverage labels, so FDA would consider a juice product sweetened with an ingredient derived from sugar cane and labeled as 100% fruit juice to be misbranded, it said. FDA would not object to the addition of one or more truthful, non-misleading descriptors before the common or usual name “sugar,” it said. “Such a descriptor, which could be a coined term, could be used to distinguish the ingredient from white sugar and other sugars on the market by describing characteristics such as source, color, flavor, or crystal size.”
On May 23 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: