Production starts when the specification is already approved
Bring an approved formula, a physical sample or a written batch standard, plus the pack plan, quantity and destination market. Compounding, filling and packing then run at the Guangzhou site. SGS ISO 22716 (CN21/31217) and US FDA Cosmetic GMP (CN21/31218) are held by Guangzhou Yuanxu Pharmaceutical Co., Ltd., valid to July 2027. Prink uses this site; the two companies are separately registered.
Bases already listed in the catalog stay on Bulk Bases. Licensing a Prink formula so your own team can reproduce it stays on Training and Formula Transfer.
Production scope
The factory compounds, fills and packs to the agreed standard
Each project confirms its own scope. The three groups below are the manufacturing work on this route.
Compounding and bulk
- Compound to the approved formula or batch standard
- Scale that standard to the planned bulk quantity
- Check materials and equipment fit before the run is committed
Filling
- Fill once the bulk matches the approved sample or written reference
- Use the pack formats confirmed for the order
- Keep the fill aligned with the packing plan
Packing and labeling
- Pack finished units for the confirmed shipment
- Apply the labeling plan agreed for the order
- Stage goods against the packing list
Production brief
Tell us the specification, pack plan and volume
Send the approved formula or standard, the target quantity, the pack direction and the destination market. We confirm whether this production route fits. The form below is the same inquiry used on the quote page.
Next path
Use another page when the brief is not ready to manufacture
These two routes prepare a standard. Come back here when that standard is approved and you need the factory to run it.
Private label skincare
Choose a proven base, apply your artwork, and plan repeat supply. You are not asking this page to develop a new formula.
View private label
Custom formulation
The formula still needs lab work: actives, texture, fragrance or color. Production moves here after you approve the batch reference.
View custom formulation
How a run moves
Four checkpoints keep the batch on the approved standard
You set the reference. The factory manufactures to it.
Share the production brief
You. Send the formula, sample or specification, target quantity, pack direction and destination market.
Factory. Log the brief against this production route.
Confirm production fit
You. Answer questions on materials, pack compatibility and timing.
Factory. Review equipment fit and costing before the run is committed.
Approve the batch reference
You. Confirm the pre-production sample or written standard.
Factory. Lock that file as the reference for the bulk order.
Compound, fill, pack and check
You. Confirm shipping details for the finished goods.
Factory. Manufacture, fill, pack and check quality against the approved standard.
Documents follow the batch record
When batch records are available, export shipments commonly include the documents buyers need for intake and compliance review.
- COA
- SDS / MSDS
- INCI
- Packing list and commercial invoice
- Technical files related to the order
Orders start at 50 kg and ship in 7–15 days
Orders start from a 50 kg MOQ and ship in 7–15 days after approval, subject to the production schedule. These are planning ranges, not guaranteed lead times.
