New York, NY—WholeFoods reported last month on the U.S. Food and Drug Administration’s (FDA) publication of draft guidelines concerning the distinction between beverages and liquid dietary supplements. Since then, as part of the commentary phase of the FDA guideline process, Ullman, Shapiro and Ullman, LLP have submitted a thorough response statement in opposition to the proposed FDA guidelines.
Buffalo Grove, IL—North American Herb and Spice (NAHS) is holding a NAHS Wild Medicine Exploration Contest until June 2010. Stores can compete in various categories (such as best display of NAHS products) for a chance to win a trip to the northernmost Canada wilderness.
Port-Au-Prince, Haiti—On Tuesday, January 12, the Port-Au-Prince region of Haiti experienced an earthquake, which ranked 7.0 in magnitude, leaving in its wake a path of destruction. For those living the disaster, the day was filled with shock, fear and total chaos. But, for the rest of the world watching, it was a time to reach out and offer hope to disaster-torn Haiti.
Washington, D.C.—The Natural Products Association (NPA), headquartered here, invites industry members to join in Natural Products Day on March 23. This free event offers an opportunity to meet Congressional representatives on Capital Hill and discuss key industry issues with legislatures.
Washington, D.C.—Former Presidential candidate, Senator John McCain (R-AZ), has introduced new legislation, the Dietary Supplement Safety Act of 2010, which will amend the current Federal Food, Drug, and Cosmetic Act (FD&C Act). In this bi-partisan bill, co-sponsored by Senator Byron Dorgan (D-ND), McCain seeks “to more effectively regulate dietary supplements that may pose safety risks unknown to consumers.”
Gainesville, FL—Data collected in November/December 2009 by resveratrol supplement maker ReserveAge Organics, based here, offer some illuminating insight into consumers’ attitudes with respect to this popular herb.
Rockville, MD—Following some 30 years of toxicology research surrounding the health threats of bisphenol-A (BPA) exposure, the U.S. Food and Drug Administration (FDA) is finally stating that there exists “some concern” for infants and children exposed to this chemical after having stated it was harmless for decades.
In a notice published in the December 4 Federal Register, the Drug Enforcement Administration (DEA) ruled that boldione, desoxymethyltestosterone (DMT) and 19-nor-4,9(10)-androstadienedione will all be classified as anabolic steroids under the Controlled Substances Act.