Washington, D.C.—The American Herbal Products Association's (APHA) Board of Trustees isn't convinced that dietary supplement makers should be required to register their products with the U.S. Food Administration (FDA) "as a stand-alone approach to improving informed consumer access to a wide variety of safe dietary supplement products."
Bethesda, MD—The Office of Dietary Supplements (ODS) has been keeping a Dietary Supplement Label Database (DSLD), and is now wondering whether to expand the resource with additional features and added functionality.
In the latest attack on the supplements industry by state attorney generals (AGs), GNC is being sued by Oregon’s AG Ellen Rosenblum, for allegedly selling supplements spiked with unmarked illegal ingredients.
A.T. Kearny released a study on October 26 detailing the growth of local food trends titled, “Firmly Rooted, the Local Food Market Expands.” The study surveyed 1,500 shoppers who indicated being the primary shopper or sharing in shopping responsibilities. The results of the survey found that the consumer definition of “local” is narrower than the accepted definition.
Researchers from the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) recently published data in the New Journal of Medicine suggesting that 23,000 emergency room (ER) visits every year were caused by reactions to dietary supplements intake. Industry groups strongly disagree with the determination that supplements are unsafe.