The United States Food and Drug Administration (FDA) typically takes regulatory action against unsafe or misbranded herbal products post-market, often only after adverse effects have been reported.

Authors

• Person: Not available Organization: Springer
  Medicinal plants and human health: a comprehensive review of ...

Sources

• Medicinal plants and human health: a comprehensive review of ... link.springer.com Springer via serper

Referenced by nodes (1)

• United States Food and Drug Administration entity