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FDA promotes mandatory listing of dietary supplements and strengthens market traceability supervision

2026-07-31

The US Congress advances the Dietary Supplement Listing Act in 2026, aiming to transform the decades‑old post‑market supervision model. All dietary supplements sold within the US shall complete mandatory FDA product listing registrationDemocrats.

Dietary supplement labeling compliance strengthened, FDA strictly controls efficacy claims

FDA continues to strengthen label supervision for dietary supplements, cracking down on disease‑treatment or‑relief claims without valid scientific evidence. Under updated requirements, all dietary supplements must clearly distinguish

The new regulations on food allergen labeling have been fully implemented, and the labeling of the eight major allergens is mandatory

US food allergen labeling regulations are fully implemented. Foods and health supplements containing food‑derived ingredients are mandatorily required to label eight major allergens: milk, eggs, fish, crustacean shellfish, tree nuts, wheat, peanuts and soybeans.

Continuous tightening of FSVP supplier verification requirements for imported food and health products

Enforcement of the US Foreign Supplier Verification Program (FSVP) is intensified. For all foods and dietary supplements sold into the US, overseas manufacturers must comply with FSVP obligations.

NAC dietary supplement regulatory policy update, some products are prohibited from sale

FDA updated its regulatory stance on N‑Acetylcysteine (NAC). Since NAC was previously approved as a pharmaceutical drug, FDA considers there are compliance barriers for selling NAC in the form of dietary supplements. Certain NAC‑containing health supplements are ruled unmarketable as dietary supplements.