Health and Healthcare
What the FDA Approves -- and What It Doesn't
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When the U.S. Food and Drug Administration (FDA) makes a decision to approve or reject a new product, that decision often dictates whether a small company will flourish or disappear. But the FDA also regulates a lot of other things, and it does not regulate a lot more.
A product advertised as “FDA-approved” may or may not have been approved by the agency, and, as in almost all marketplace decisions, it’s buyer beware of these claims.
The FDA does, of course, review and approve new drugs and some biologics, but most are not labeled as “FDA-approved” because prescription drugs cannot be marketed in the United States without FDA approval. When it approves a new drug, that means the agency has reviewed all the testing done by the manufacturer and determined that the benefits of the drug outweigh known risks for the intended use of the drug. The FDA does no testing of its own.
Here are some other things that do require FDA approval before being sold:
If you see the words “FDA-approved” in relation to or advertising for these products, you might want to check to see if the claim is true. The FDA’s logo is for official use only and may not be used to suggest that the agency endorses a company, a product or a service.
Here are products and services the FDA does not routinely review or approve:
Check the FDA’s consumer updates page for more details and other consumer information from the FDA.
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