Capabilities
Everything that decides whether your product arrives identical to the sample happens here: the lab, the lines and the release bench. Nothing is subcontracted.
01 — Formulation
Cushion, concealer, lip and powder behave nothing alike. Each category has its own formulator, so the person matching your shade also knows how that bulk will fill, set and travel.
5,000+ validated bases mean most projects start from a formula that already passed stability and compatibility testing, rather than from zero.
| Laboratory | 2,000 m² independent formulation and testing space |
| Formulators | Dedicated formulator per product category |
| Formula library | 5,000+ validated bases across colour cosmetics |
| Shade library | 500+ shades already matched and on file |
| Sampling | Physical samples in 3 days from brief |
02 — Production
Powder, paste and liquid run as separate lines with their own equipment and their own operators — because the tolerances are not interchangeable.
Pressed powder, blush and highlight. Pan pressure is held constant across the run so density — and therefore payoff — does not drift between the first and last hundred pieces.
Lipstick and stick formats. The cooling curve is controlled to limit pinholes, surface sink and sweat, which is where most bullet rejects come from.
Automatic servo filling for tube and bottle. Cushion compacts use vacuum adsorption filling — the step that decides whether the puff draws an even dose or a wet patch.
03 — Quality control
Five layers sit between incoming material and the shipping carton. Each has an owner and a record.
| Layer | What happens | Record |
|---|---|---|
| Incoming material | Identity and specification check on every raw material and component lot | Incoming inspection sheet |
| First piece | First filled unit of each run approved against the standard before the line continues | First-article approval |
| In-process | Interval checks on fill weight, colour and appearance during the run | In-process log |
| Release testing | The five batch tests below, on every batch | Batch test report & COA |
| Retention | Retained sample per batch, held for traceability and complaint investigation | Retention register |
| Test | Measured on | Fails when |
|---|---|---|
| Colour difference | ΔE against approved standard | The shade drifts outside tolerance |
| Particle size | D90 of milled powder | The powder reads gritty or pays off unevenly |
| Melting point | Drop point of paste bulk | The bullet or pan softens in transit |
| 1.2 m drop | Packaging and pan after drop | The compact cracks or the case opens |
| Microbiological | Seven standard tests | Any result outside specification |
04 — Compliance & documentation
A product can be perfect and still be stopped at the border by a missing document. We release the technical file with the batch, not on request afterwards.
Our facility is registered with the U.S. FDA. For the EU, we supply the technical documentation your Responsible Person needs to compile the Product Information File and notify through CPNP.
| Licence | Cosmetic production licence 粤妆20230139 |
| U.S. market | FDA-registered manufacturing facility |
| EU market | Technical documentation for your Responsible Person |
| Per batch | COA, batch test report, retention sample record |
| Per formula | INCI list, specification sheet, MSDS |
| On request | Stability, microbiological and heavy-metal reports |