What is one of the FDA's roles in supplement manufacturing?

The role of the FDA in supplement manufacturing primarily involves ensuring that products are safe and accurately labeled, rather than approving marketing materials outright. The FDA does not maintain a database specifically for contaminated supplements, but it does monitor the safety of dietary supplements once they are on the market and can take action if a product is found to be harmful or falsely labeled.

The FDA plays a critical role in regulating the safety and labeling of dietary supplements, which includes reviewing reports of adverse events and taking necessary regulatory action to protect public health. While it does not actively control prices or specifically regulate supplements aimed at enhancing athletic performance, its oversight is crucial in ensuring that all dietary supplements meet safety standards before they reach consumers.

Thus, while the given answer refers to the FDA's role in overseeing safety, it's important to note that the FDA does not maintain a specialized database for contaminated supplements, although it does react to safety issues as they arise in the broader context of dietary supplement regulation.