Zhejiang Medicine Company, Ltd. (ZMC), Zhejiang Province, China, has received verification from the U.S. Pharmacopeia (USP) that the company’s D-alpha tocopheryl succinate, D.L alpha tocopheryl acetate and D-alpha tocopheryl acetate ingredients are in compliance with the USP Ingredient Verification Program. USP based its decision on three factors: a GMP audit conducted at the company’s facilities; a review of the manufacturing and quality control/quality assurance documentation; and laboratory testing. The USP verification of ZMC manufactured vitamin E ingredients assures the ingredients are consistent in quality from batch to batch; meet label or certificate of analysis claims for identity, strength, purity and quality; and are prepared in accordance with accepted manufacturing processes.