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.
- Yes.
- For U.S. buyers we can provide a batch-specific Certificate of Analysis (COA) for each production lot, aligned to the specifications you confirm during sample approval.
- Each COA typically includes product name/SKU, batch (lot) number, manufacturing date, QC release date, specification limits, test items and results, and QC sign-off for traceability.
- Key COA items are set by your spec, but commonly cover organoleptic checks (appearance/color/odor), basic phys-chem and stability-related checks used in our QC, plus pass/fail versus agreed limits.
- If you need additional documentation or third-party testing, we can arrange sample submission and follow up inspection reports as part of our testing support (we do not guarantee regulatory approval, but we support documentation and testing workflows).
- MOQ depends on your formula and packaging (bottle type and pack components); we confirm after scientific product selection and方案确定.
- Lead time: bulk production is typically 10-20 working days after final sample approval; packaging orders usually take 10-30 working days (e.g., glass bottle ~15 days, acrylic bottle ~30 days; single box ~15 days, set box ~20 days).
- We also support formula customization and sampling, VI/packaging design, barcode/required certificates support, and end-to-end delivery logistics.
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.
