Explore our market-tested base formulations engineered for superior cutaneous absorption, skin barrier repair, and stability under varied climatic environments.
The international skincare industry has reached an inflection point where clean label credentials must intersect with provable clinical bio-availability.
Traditional petrochemical emulsions are rapidly being superseded by biomimetic lamellar gel networks. Modern consumers demand lipid phases mimicking physiological stratum corneum matrices—leveraging phytoceramides, non-hydrogenated squalane, and fermented seed lipids to rebuild damaged skin barriers without occlusive pore clogging.
The phase-out of parabens and isothiazolinones led initial brands into unstable organic acid solutions. Today’s state-of-the-art relies on multifunctional anti-microbial glycols, caprylyl glycol isomers, and fermented radish root or lactobacillus filtrates that preserve product integrity across 36-month shelf lives without destabilizing cutaneous flora.
Brands can no longer rely on 'fairy dusting' botanical extracts. Our private label development aligns plant extracts with functional clinical benchmarks—stabilized vitamin C derivatives, bakuchiol as a gentle bio-retinoid alternative, and multi-molecular hyaluronic matrices ensuring immediate barrier quenching alongside deep dermal hydration.
Operating Guangzhou Aoyan Cosmetics Co., Ltd. and Guangzhou Xinzimei Cosmetics Co., Ltd., we eradicate broker premiums through direct, transparent production pipelines.
Formulation built around custom client requirements, specific regional ingredient blacklists (e.g., EU Annex II/III, Sephora Clean), rheological profiles, and skin absorption kinetics.
Sourcing and compatibility screening of airless pumps, frosted glass jars, mono-material recyclable PP/PET containers, and precision dropper assemblies to prevent active oxidation.
Comprehensive analytical testing ensuring finished goods comply with domestic and overseas safety regulations prior to dispatch, eliminating detention risk at international ports.
From low initial trial runs for direct-to-consumer digital brands to automated multi-ton filling runs for multi-door supermarket distribution networks.
Navigating the complexities of global cosmetic safety guidelines with complete documentation, testing frameworks, and export-ready credentials.
Full alignment with the Modernization of Cosmetics Regulation Act (MoCRA). Our facility provides registration numbers, professional Product Listing dossiers, safety substantiation records, and cGMP compliance assurance under ISO 22716 guidelines.
Full support for European Cosmetic Regulation (EC) No 1223/2009. We assist European brands and their Designated Responsible Persons (RP) in drafting comprehensive Product Information Files (PIF) and safety evaluations.
Compliance documentation tailored for the Gulf Cooperation Council (GSO standards), Saudi Food and Drug Authority (SFDA/SASO conformity certificate), and regional ASEAN cosmetic directives.
A disciplined, transparent 5-stage lifecycle managing formulation development, regulatory checks, packaging compatibility, and batch filling.
Evaluation of brand requirements, target market regulations, required functional actives (peptides, ceramides, niacinamide), packaging formats, and target landed unit economics.
Generation of customized bench samples for sensory evaluation, skin absorption feel, texture testing, fragrance profile refinement, and initial packaging compatibility checks.
Finalizing the approved benchmark sample. Generating the complete INCI ingredient breakdown, certifying primary bottle artwork, and pre-filing customs regulatory documentation.
Sterile vacuum emulsification, computerized high-shear blending, multi-stage filtration, and inline viscosity inspections executed in GMPC/ISO 22716 cleanrooms.
Batch-level micro-enumeration checks, heavy metal tests, issuing Certificate of Analysis (COA), export custom clearance documentation, and ocean, rail, or air fulfillment.
Our joint R&D initiatives with world-leading raw material houses ensure your brand remains at the forefront of cosmetic biochemical engineering.
Unstable natural actives such as resveratrol, ubiquinone (CoQ10), and retinaldehyde degrade quickly when exposed to oxygen and light. We utilize phospholipid bilayer nano-capsules that protect active molecules through filling and storage, releasing them across deep epidermal layers upon cutaneous application.
Fermented botanicals yield higher concentrations of micronutrients, peptides, and bio-available amino acids while dramatically reducing molecular weight. By fermenting plant inputs such as camellia sinensis, rice broth, and tremella fuciformis, we create deeply penetrating hydrators that elevate natural cream performance.
Transitioning toward low-carbon footprint beauty, our manufacturing engineers have formulated cutting-edge cold-process natural face creams. Eliminating energy-intensive heating cycles protects heat-sensitive botanical antioxidants while lowering the environmental impact of your supply chain.
From bio-cellulose treatment masks and restorative facial lotions to advanced cosmeceuticals, manufactured under certified GMPC/ISO environments.
Answers to critical questions regarding private label skincare minimums, formulation IP, lead times, stability testing, and regulatory certifications.
OEM (Original Equipment Manufacturing) entails producing a face cream precisely according to your proprietary formulation, bill of materials, and manufacturing process instructions. ODM (Original Design Manufacturing) leverages our established library of over 3,500 clinically tested, commercially stable base formulations, which can be tailored with specific botanicals, proprietary scents, and branded containers to reduce lead times significantly.
Our dual production facilities in Guangzhou operate under strict international compliance standards, holding GMPC (Good Manufacturing Practice Cosmetics for both US FDA and European markets) and ISO 22716 certifications. We also maintain BSCI social compliance audit certifications, FDA cosmetic facility registrations, and supply fully compliant batch COA and MSDS documentation.
We utilize a multi-hurdle antimicrobial strategy combining multifunctional booster glycols (e.g., Pentylene Glycol, Caprylyl Glycol), bio-ferment filtrates, and chelating agents (such as Sodium Phytate). Every cream passes rigorous 3-month accelerated stability testing (incubated at 4°C, 25°C, 45°C, and 50°C), freeze-thaw challenge cycles, and USP 51/ISO 11930 microbial challenge tests before batch sign-off.
For existing, proven formulations utilizing standard stock packaging components, our private label MOQs can start as low as 1,000 to 3,000 units. Bespoke custom-molded packaging, silkscreened containers, or fully proprietary chemistries typically require 5,000 to 10,000 units. Standard production lead times run approximately 25 to 35 business days following final component delivery and artwork sign-off.
Yes. Our internal regulatory documentation team supplies comprehensive ingredient declarations (INCI breakdowns with exact raw material CAS numbers), finished product toxicological profiles, Certificate of Analysis (COA), IFRA fragrance compliance certificates, and stability reports necessary for your safety assessor to issue a CPSR (Cosmetic Product Safety Report) and complete CPNP notification or US MoCRA product listing.
We welcome direct factory visits or audits by third-party inspection agencies (such as SGS, Intertek, or Bureau Veritas). Our facilities feature dedicated viewing galleries, Class 100,000 cleanroom manufacturing environments, automated batch mixing suites, and comprehensive wet chemistry and microbiology analytical testing laboratories.
