We Formulate Safe, Effective
With laboratories and offices in Yunfu and Foshan, Guangdong, our team of 10+ chemists and formulation scientists develops toothpaste, mouthwash, and oral spray formulations that meet global quality standards — from concept to compliance-ready batch.
Every Formula Tested Before It Reaches Your Customer
Our testing protocol is structured in two stages — sample-stage and bulk-production stage — so issues are caught early, not after tooling or production investment.
Sample Stage Testing
- –3-day accelerated stability test
- –pH measurement (toothpaste 6.5–8.0 / mouthwash 4.5–7.0)
- –Viscosity verification (rotational viscometer)
- –Colour comparison (spectrophotometer)
- –Organoleptic evaluation — scent, texture, appearance
Bulk Production Testing
- –3-month real-time stability test (ICH Q1A)
- –Microbial testing (ISO 21149 / ISO 11930)
- –Packaging compatibility testing
- –COA, SDS & full compliance documentation
Third-Party Lab Testing (via Partner Labs)
- –Heavy metal testing — ICP-MS (SGS / Intertek)
- –Fluoride content testing — ISE method
- –Packaging compatibility (HDPE / PET / aluminium tube)
Compliance Documents Included
- –Certificate of Analysis (COA)
- –Safety Data Sheet (SDS)
- –Stability test reports
- –CPSR support for EU / UK market registration
Formulated for Your Market.
Documented for Your Regulator.
We work closely with a cosmetic R&D and regulatory team based in the United Kingdom to develop formulations that comply with both China's NMPA regulations and the EU Cosmetics Regulation (EC No 1223/2009). This dual-track approach means your product is ready for both Eastern and Western markets from day one.
When your brand is ready to register locally, we provide the full technical documentation package your regulatory consultant will need — including formulation disclosure, ingredient safety data, stability reports, and manufacturing site information.
Ask About Compliance SupportChina NMPA
Cosmetics registration documentation and formulation compliance for the Chinese market.
EU Cosmetics Reg.
EC No 1223/2009 compliant formulations. CPSR-ready safety assessment documentation.
US FDA
Cosmetic and OTC monograph guidance for fluoride toothpaste (21 CFR Part 355).
UK CPSR
UK-specific cosmetic product safety report support via our UK-based R&D partner team.
Three Ways to Develop Your Oral Care Formula
Whether you need a fully custom formula built from scratch, a fast-track modification of an existing base, or a proven ready-to-go formula — we have a development path that fits your timeline and budget.
Efficiency and Rigour.
Never One Without the Other.
Our streamlined development process supports fast iteration and flexible production without compromising on compliance or quality.
Fast Iteration
From brief to sample in as little as 7–14 days for standard formulas.
Regulatory Rigour
NMPA, EU, and US FDA compliance built into every formula from the start.
Professional Chemistry Team
Chemists with 20+ years of oral care formulation experience.
Sustainability-Forward
Waterless toothpaste tablets, solid paste formats, and eco-friendly packaging options.
A Stable 10% Nano-Hydroxyapatite Toothpaste, Ready to Scale
Nano-hydroxyapatite (nHA) is one of the most technically demanding oral care actives to formulate at a clinically relevant concentration. After multi-batch R&D and accelerated stability testing, our team has a production-ready 10% nHA toothpaste formula — validated, documented, and available for private label.
Common Questions About Our Formulation Services
Can't find what you're looking for? Our team responds within 24 hours.
Ask a QuestionInnovations Proven by Patents








Trusted By Oral Healthcare Brands













