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.
- For US sunscreen imports, we provide comprehensive documentation including Certificate of Analysis (COA) with active ingredient concentrations, pH, and viscosity measurements.
- Safety Data Sheets (SDS/MSDS) detail composition and handling protocols.
- Stability reports include real-time and accelerated testing at 25°C/60%RH and 40°C/75%RH with 3-month intervals.
- Microbial testing covers total aerobic count, yeast, mold, and E. coli with <100 CFU/g limits.
- We also provide FDA registration support and CPSC compliance documentation.
- For MOQs of 5,000 units, documentation is included in sampling timeline of 4-6 weeks.
- Packaging compliance includes SPF testing and water resistance validation.
- Lead time for full documentation package is 2 weeks post-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.