FDA Proposes New Policy to Target Certain Homeopathic Drugs

On December 18, 2017 the U.S. Food and Drug Administration (FDA) released a new proposed policy targeting unapproved drug products labeled as homeopathic that have the greatest potential to cause risk to patients. According to the FDA’s Web site, the new approach aims to protect consumers who choose to use homeopathic products, by updating the FDA’s existing policy to better address situations where homeopathic treatments are being marketed for serious diseases and/or conditions but where the products have not been shown to offer clinical benefits.