ISO 22716 & GMPC · Certified by Intertek
View certificatesGZ Cosmetics Lab is a cosmetics contract manufacturer in Guangzhou, China, providing OEM, ODM, private label and custom formulation for skincare, sun care, hair care, body care and aromatherapy brands. We coordinate formula development, sampling, production, packaging, quality documentation and project-specific testing support.
Supramolecular delivery options are assessed when they suit the formula; any licensed technology or patent reference is confirmed per project.
A CDMO scope can combine ingredient registration support, patent-filing support, regulatory documentation, and manufacturing, with external parties defined up front.
Stated daily capacity across 13 lines and 20 product categories, scheduled against the confirmed production plan.
Ingredient options from suppliers such as BASF, Symrise, and Croda are reviewed for the formula and required documentation.
The Problem
Generic OEM means generic results. Your customers notice. Where the formula calls for it, an advanced delivery system can help keep actives stable and evenly distributed rather than separating out, confirmed by stability data for your formula. That's the difference between a product that sells once and one that builds a brand.
How We Work
Whether you have your own formula or need us to develop everything from scratch.
You provide the formula. We manufacture to an agreed specification with the order documentation confirmed for the project.
We develop the formula from your brief. Ownership, permitted use, confidentiality, and any exclusivity follow the signed agreement.
Select an existing catalogue formulation to reduce development work. MOQ and timing are confirmed for the chosen product and packaging.
One coordinated programme — formulation development, ingredient registration and patent-filing support, regulatory documentation, and production.
What We Make
Skincare, body care, hair care, and aromatherapy — all manufactured in our GMPC production base.
Featured Products
A selection of ready-to-brand product directions, from brightening serums to sunscreen formats.
Amino acid + Centella gentle cleanser for daily use.
View productBrighteningHigh-purity glutathione + niacinamide for even tone and radiance.
View productRepair92% snail secretion filtrate that hydrates and supports the skin barrier.
View productHydrationMulti-weight hyaluronic acid for deep, layered hydration.
View productSun CareLightweight aqua-texture sunscreen for tropical climates.
View productBody CareNiacinamide body lotion for smooth, even-toned skin.
View productHair CareNatural botanical shampoo for scalp balance and shine.
View productFragranceFresh tropical fragrance, private label ready.
View product
Why We're Different
Our advanced supramolecular delivery platform can be considered when it suits the formula. Performance targets, specifications, and supporting tests are confirmed for the project.
Why Brands Choose Us
Review the production, quality, and development capabilities that can be matched to your project.
The standard starting point for many bottled or jarred products. Final MOQ depends on the formula, dosage form, raw materials, filling process, and packaging components.
Bulk production after the approved sample, packaging, and order details are confirmed. Special formats and testing are scoped separately.
Existing-formula and custom ODM sample schedules are confirmed after the brief, reference information, formula route, and courier destination are clear.
13 production lines provide capacity for both confirmed production minimums and higher-volume orders, subject to the agreed production plan.
ISO 22716, GMPC, ISO 9001, ISO 14001, HALAL, ISO 45001. SGS testing supported upon request. Documentation support for US, EU, ASEAN, and Middle East exports.
Advanced supramolecular delivery technology is available under license when it suits the formula and agreed development scope.
How We Work
Illustrative examples of how projects run with us. These describe our process and capabilities, not the results of any specific client engagement.
A brand arrives with an existing vitamin C serum that needs reformulating onto a delivery system suited to its actives. The work is specification-driven: agree the target texture and actives, then define the development screening and any formal stability work required before production.
A brand moving production to us runs the transfer as a controlled changeover. Batches are produced under ISO 22716 and GMPC on our 13 lines, with in-process checks and batch testing against the agreed specification at every step.
A brand needing more than manufacturing agrees a CDMO scope that can include ingredient registration, patent-filing support, formulation development, a testing plan, and regulatory documentation ahead of launch.
Trusted By
Beauty and personal care brands from Asia, Europe, and North America manufacture with us.
Where You Sell
A GMP certificate is not a market entry. Your destination country sets the notification route, the labelling rules, whose halal certification counts, and which claims you can make. It often changes the texture buyers will accept. Tell us the market early and we will confirm what is in scope before you pay for a sample.
Indonesia · Thailand · Vietnam · Philippines · Malaysia · Singapore
One regional directive, six separate notifications, six authorities, plus the tropical formulation choices that decide whether a product sells.
See the market page →
GCC states · UAE · Saudi Arabia
GSO conformity, halal certification recognised by the importing state, and Arabic labelling.
See the market page →
EU 27 · United Kingdom
CPNP notification, a Responsible Person inside the market, and a PIF needing a GMP statement from the actual site.
See the market page →
MoCRA
Facility registration by us, product listing by you. No FDA approvals or certificates exist for cosmetics.
See the market page →
See all export markets·Registration is filed by a local entity in most markets, not by the factory. We are explicit about which parts stay with you.
Inside Our Facility
From raw materials to finished goods — everything happens in our GMPC-certified facility in Guangzhou. Factory visits welcome.
Resources
Decide whether to build, which model fits, and what it really costs.
Compare regions and vet the right OEM partner with confidence.
Register and launch across every Southeast Asian market.
Category playbooks and the actives driving today's best sellers.
Common Questions
Our MOQ starts from 3,000 units per SKU depending on the product and level of customization. Most skincare (creams, serums, lotions) and body care sit at 3,000 units per SKU; some formats are higher, such as sheet masks and collagen patches at 5,000 to 10,000 sheets depending on material and packaging. We confirm the applicable minimum before quotation.
Sample preparation, dispatch, courier transit, and revision rounds are confirmed for each project after the brief, formula route, reference information, and destination are clear. Existing formulations usually require less development work than a custom ODM formula.
We hold ISO 22716 (Cosmetics GMP, certificate HBPCER20260352) and GMPC (HBPCER20260353), both issued by Intertek and valid to 15 July 2029, plus ISO 9001, ISO 14001, ISO 45001, HALAL certification, and US FDA facility registration under MoCRA (FEI 3038966060). We also hold a valid Chinese cosmetics production license. The Intertek certificates can be verified directly at certs.intertek.com.cn. SGS testing is supported upon request. These certifications support the documentation typically required for US, EU, ASEAN, and Middle East markets; final compliance also depends on your formula, labelling, and registration route.
Yes — this is our core strength as a CDMO. We develop formulations from concept to production-ready, specializing in advanced actives (PDRN, Ectoin, exosomes, peptides) and our licensed advanced delivery system. Development typically takes 4–8 weeks including stability testing.
Verify Before You Buy
Use the evidence pages below to check certificates, testing boundaries, production fit, quality controls and the documents or audit questions relevant to your project.
See what a usable test plan and report should contain.
Review evidence →Check certificate numbers, scope and independent verification routes.
Review evidence →Match formula, packaging and volume to usable line capacity.
Review evidence →Follow controls from incoming materials to shipment release.
Review evidence →Open available certificate and facility-registration documents.
Review evidence →Prepare an onsite, remote or third-party supplier review.
Review evidence →Share your product brief. Our technical team responds within 24 hours with a quotation or the questions needed to prepare one.
