Why does the FDA regulate medicines and the information on medicine labels?

The FDA regulates medicines and their labels to ensure public safety and efficacy, ensuring that products are safe for consumption and effective for their intended uses. This regulation helps prevent misleading claims and ensures that consumers have access to accurate information about potential side effects, dosage, and proper usage. By overseeing the approval process and labeling standards, the FDA aims to protect public health and promote informed decision-making regarding medications.