​Is Herbalife FDA-approved?​

Herbalife strictly follows all FDA regulations as they apply to dietary supplements under the Dietary Supplement Health and Education Act (DSHEA). These regulations establish guidelines for product quality, labeling and ingredient safety – standards that Herbalife is fully committed to meeting.

However, it’s important to understand that the way the FDA regulates dietary supplements is different from how it regulates prescription drugs or over-the-counter medications. Under current regulations, the FDA does not have the authority to approve dietary supplements for safety or effectiveness before they reach the market. Instead, it is the responsibility of manufacturers like Herbalife to ensure that nutrition products meet regulatory standards governing their content, manufacturing and labeling.

Has the FDA banned Herbalife?

No, Herbalife has never been banned by the FDA. The company complies with all applicable U.S. food and supplement regulations.

Does the FDA regulate Herbalife?

Yes, the FDA oversees dietary supplement regulations, including labeling and manufacturing practices, but it does not “approve” supplements before they go to market. Unlike prescription drugs, which require FDA approval based on clinical trials, dietary supplements are monitored for safety and compliance through post-market regulation.

To maintain high-quality standards, our Herbalife24 line of products undergo independent testing and third-party certification for sports by NSF International, a global product safety organization. Herbalife also follows strict internal safety processes, including DNA testing and chemical analysis to verify botanical ingredients and third-party audits of vendor facilities.

For more details on FDA dietary supplement regulations, visit the official FDA website.