Yes, the US Food and Drug Administration regulates dietary supplements, but the framework is different from that of conventional food and drugs. Dietary supplements are considered a category of food, and as such, the FDA does not approve them before they reach the market. Instead, manufacturers are responsible for ensuring that their products are safe and that labeling is truthful and not misleading. This means that while the FDA does monitor the market for dietary supplements, it primarily steps in when there are safety issues or claims of disease treatment or prevention that are not substantiated. The law also requires that dietary supplements bear a Supplement Facts label, which provides consumers with information about the product's contents. Individuals interested in dietary supplements should check the FDA's official website for detailed guidance and information on specific products, as the agency actively provides resources related to dietary supplements and their safety.