Quick Answer (for busy buyers)
Here’s the buyer-first summary. If your brand name is on the label, you usually act as the responsible person and must ensure the listing is submitted and kept current.
- U.S. skincare labels require INCI names precisely as listed in the International Cosmetic Ingredient Dictionary, with ingredients in descending order of predominance.
- Common mistakes include using trade names instead of INCI names, incorrect capitalization, or grouping ingredients.
- We verify all labels against the latest FDA database during sampling and provide documentation for compliance.
- For US market entry, we recommend starting with 500-unit MOQ for label testing, which adds 7-10 days to sampling timeline.
- Our QA team conducts label mock-ups with actual packaging to check for legibility and regulatory alignment before production.
Buyer outcome
A launch-ready compliance plan: inputs collected, roles assigned, and update cadence defined.
Most common blocker
Missing facility information + inconsistent ingredient/label snapshots across SKUs.
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This page is a practical buyer guide. For definitive requirements and updates, use FDA resources and qualified regulatory counsel.
