US SB3677

Requires all dietary supplement manufacturers, packers, or distributors to register their products with the FDA, including product name, ingredients with amounts per serving, label copy, health claims, allergen statements, and contact information for the responsible party

Existing supplements on the market before January 1, 2027 must be listed within 18 months of enactment; new supplements must be listed at the time of introduction into interstate commerce

FDA must establish a publicly searchable electronic database within 2 years containing listing information, while keeping certain business contact details and proprietary blend ingredient amounts confidential

Dietary supplements failing to comply with listing requirements would be deemed misbranded, and products handled by debarred persons are prohibited from interstate commerce

Authorizes $7,872,984 for fiscal year 2026 and $6,615,000 annually for fiscal years 2027-2030 to implement the listing program and hire necessary personnel