Downloadable data files. FDA Adverse Event Reporting System (FAERS) Public Dashboard Inactive Ingredient Search for Approved Drug Products Search More information Medication Guides Search More. FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other notifications. FIS has been. What Does FDA Do? Each day in America, you can trust the foods you eat and the medicines you take, thanks to the U.S. Food and Drug Administration. The FDA has added bemotrizinol as an active ingredient for use in sunscreens, supporting greater consumer choice for safe and effective sun protection products. Read more about this new ingredient The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the. Contact Us Food and Drug Administration Food and Drug Administration White Oak Campus 10903 New Hampshire Ave Silver Spring, MD 20993 United States Primary 1-888-INFO-FDA 1-888-463-6332 The Food and Drug Administration (FDA) is an HHS agency that regulates clinical investigations of products under its jurisdiction, such as drugs, biological products, and medical devices. The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs. The regulation of food and dietary supplements by the Food and Drug Administration is governed by various statutes enacted by the United States Congress and interpreted by the FDA.