The U.S. Food and Drug Administration regulates:

Question

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The U.S. Food and Drug Administration (FDA) is responsible for regulating the labeling of all prescription and over-the-counter drugs to ensure they meet safety and efficacy standards. This includes overseeing the information provided on drug labels, which must accurately describe the drug's uses, dosage, warnings, and other critical information for consumers and healthcare providers. The FDA does not regulate the practice of medicine, such as prescribing drugs by medical professionals or making off-label recommendations, nor does it oversee pharmaceutical educational offerings directly.

The U.S. Food and Drug Administration Regulates