Zhejiang Medicine Co. Ltd.

THE WOODLANDS, Texas—Zhejiang Medicine Co. (ZMC; ZMC-USA.com) announced its USP-grade ingredients D-alpha tocopheryl succinate, D.L alpha tocopheryl acetate and D-alpha tocopheryl acetate have been found to be in compliance with the requirements of the USP (United States Pharmacopeia) Ingredient Verification Program.

USP based its decision to grant this determination of quality based upon three factors; (a) a good manufacturing practices audit conducted at the site noted above; (b) a review of the manufacturing and quality control/quality assurance documentation; and (c) 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;

• Are prepared in accordance with accepted manufacturing processes.