Categorized as dietary supplements by the U.S. Food and Drug Administration (FDA), herbal products sold here are subject to different regulations than those applied to the pharmaceutical industry. As the U.S. market for these products continues to expand, it’s becoming increasingly vital for supplement manufacturers and distributors doing business here to master the evolving regulatory landscape. This overview of current requirements will help herbal medicine providers take the first step toward winning the trust of discerning American consumers by offering traditional Ayurvedic formulations that consistently comply with FDA safety and quality standards.