FDA Compliance: How iHerb-Associated Products Fit U.S. Regulations

Understanding FDA Regulation of Supplements

In the United States, dietary supplements are regulated under the Dietary Supplement Health and Education Act (DSHEA).

Supplements are not FDA-approved before sale, but must comply with:

• Good Manufacturing Practices
• Proper labeling
• Ingredient safety standards

Does iHerb Follow FDA Rules?

iHerb, as a U.S.-based retailer, distributes products manufactured under applicable regulations.

For the headquarters background check iHerb headquarters page.

Manufacturer Responsibility

Under U.S. law, manufacturers — not retailers — are primarily responsible for:

• Product safety
• Ingredient accuracy
• Label compliance

However, retailers may require suppliers to meet compliance standards.

International Compliance

For international shipments, products must also meet the import regulations of destination countries.

FDA vs Pharmaceutical Approval

Supplements are not approved like prescription drugs. Consumers sometimes misunderstand this distinction.

Understanding this regulatory framework helps answer safety concerns often raised in.

Summary

iHerb distributes supplements that must comply with applicable U.S. manufacturing and labeling regulations. FDA oversight applies to manufacturing standards rather than pre-sale product approval.