The question buyers ask most is not "can you make it" but "does this actually count as Vietnamese". This page covers the plant location, origin rules, how access differs across three markets, and exactly what the China-side team does. We do not print specific tariff rates — they move, and only a line-by-line HS lookup counts.
| Where it is made | Lot 48, Tan Duc IP, Tay Ninh, Vietnam — every production step happens here, with no third-country subcontracting |
|---|---|
| Plant & lines | 15,000 sqm, 24 production lines; emulsifying tanks 14.9 t per batch, 39 t/day |
| Port of export | FOB Cat Lai (Ho Chi Minh City) |
| Certificates | ISO 9001:2015 (749435, valid to 2027-08-17) · CGMP-ASEAN (912/GCN-QLD, renewal in progress) · US FDA facility registration (FEI 3030839348, registration expired 2026-05-31) |
| China-side role | Sales, quoting, technical and content — no production step. There is no "made in China, relabelled in Vietnam" path here. |
Filling alone does not change the HS code. Shipping finished bulk from China into Vietnam to be bottled usually does not constitute substantial transformation — to US CBP it is still Chinese origin. We do not take that route.
Substantial transformation needs at least three things: the bulk is compounded in Vietnam (not imported ready-made), packaging is local or third-country (Vietnam self-supply is thin — this is the biggest lever), and the BOM and process are traceable.
We do not guarantee clearance on your behalf. Origin is determined by the importing customs authority, not the factory. What we provide is process records, BOM, COO and test reports for your declaration.
| Market | Tariff structure | Compliance route | What we can provide today |
|---|---|---|---|
| ASEAN (Thailand / Philippines / Malaysia / Vietnam) | Preferential treatment under ATIGA | ASEAN Cosmetic Directive framework; national notification differs by country. Indonesia additionally requires MUI Halal certification | CGMP-ASEAN, COA, COO; Indonesian orders not taken — that certification is not held yet |
| European Union | 97% of categories move to zero duty under EVFTA | CPNP notification + CPSR safety report + EU responsible person | CGMP-ASEAN, COA, test reports; CPNP / CPSR / responsible person must be handled by the importer or its agent |
| United States | MFN rate plus Section 301 and other additional measures (rates change — verify HS line by line) | MoCRA facility registration and product listing; sunscreen falls under drug rules | FDA facility registration (FEI 3030839348 — a filing, not an approval; expired 2026-05-31), COA; we do not take sunscreen orders |
The tariff column gives structure only, not numbers. Send an HS code for specifics.
You get three answers back: whether it is feasible, the MOQ, and how sampling works. If it does not fit our lines, we say so in the first email instead of the third meeting.