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 import and retail, we supply comprehensive documentation including Certificate of Analysis (COA) with batch-specific results, Safety Data Sheet (SDS/MSDS) compliant with OSHA standards, and 3-month stability reports at 25°C/60% RH.
- Our microbial testing includes total aerobic count, yeast, mold, and pathogen screening.
- MOQ starts at 5,000 units per SKU, with sampling timeline of 4-6 weeks.
- Lead time for production is 8-10 weeks after approval.
- We can support additional testing as needed for your specific claims.
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.