Search Results for 'FDA'

The United Natural Products Association (UNPA) commended FDA action to recall five products illegally marketed as sports enhancing dietary supplements. Read More »

As FDA continues to focus on steroids in supplement products, Bodybuilding.com, LLC is recalling all lots and expiration dates of 65 dietary supplement products sold through the company's website. Read More »

FDA has sent a warning letter to Procter & Gamble notifying the company that its Vicks DayQuil Plus Vitamin C and Vicks Nyquil Plus Vitamin C are illegally marketed combinations of drug ingredients and a dietary ingredient. Read More »

FDA and WebMD Health Corp. have expanded their partnership to provide increased access to FDA's consumer health information. Read More »

Joshua Sharfstein, MD, principal deputy commissioner of FDA, offered remarks at the Council for Responsible Nutrition Annual Conference, saying the agency and the industry must continue working together to protect consumers. Read More »

FDA has warned consumers to use extreme care when purchasing any products over the Internet that claim to diagnose, prevent, treat or cure the H1N1 influenza virus. Read More »

The American Herbal Products Association (AHPA), Silver Spring, MD, has suggested to FDA that the agency apply its enforcement program regarding fraudulent 2009 H1N1 products to illegal synthetic steroid products. Read More »

Final guidance from FDA regarding adverse event report (AER) labeling for dietary supplements requires either a domestic phone number or a three-line address by September 30, 2010, according to a recently published notice. Under the Dietary Supplemen… Read More »

The advent of risk factors in children/teens for serious health conditions—and their increasing recognition by parents, health professionals and the media—are driving a new, diverse and fast-emerging market opportunity as yet untapped by the functional food and dietary supplement industries. Read More »

FDA’s guidance regarding adverse event report (AER) labeling for dietary supplements requires either a domestic phone number or a three-line address by Sept. 30, 2010, according to a notice published Sept. 1. Read More »

In early August, FDA Commissioner Margaret Hamburg, MD, outlined her commitment “to prevent harm to the American people” through swift, aggressive and effective enforcement of FDA laws and regulations. Read More »

CRN, Washington, D.C., has offered comments to FDA regarding economically motivated adulteration, saying the problem is “a serious and growing concern for all consumer products industries.” Read More »

FDA action has led to the recent recall of several male enhancement products sold by two separate companies. Read More »

FDA has issued a guidance document for industry regarding adverse event reporting (AER) and recordkeeping for dietary supplements required under the Dietary Supplement and Nonprescription Drug Consumer Protection Act. Read More »