Explore eight of our benchmark skincare and body formulations, engineered with bio-compatible actives, stable micro-emulsions, and custom-tailored packaging for retail and professional spa chains worldwide.
Operating from Huadu District, Guangzhou—the epicenter of global cosmetics processing—Guangzhou Beaza Biotechnology Co., Ltd. controls the full vertical supply chain across our two dedicated manufacturing subsidiaries: Guangzhou Aoyan Cosmetics Co., Ltd. and Guangzhou Xinzimei Cosmetics Co., Ltd.
China synthesizes over 60% of the world's high-purity cosmetic actives, including synthetic Tranexamic Acid, α-Arbutin, and Ethyl Ascorbic Acid. By procuring precursors direct from molecular synthesis plants within a 50km radius, our factory eliminates cross-border logistics premiums, tariffs, and intermediary markups, offering brand partners unmatched unit-cost advantages.
Our plants operate Class 100,000 cleanroom environments conforming stringently to ISO 22716 and US FDA GMPC guidelines. With German-engineered homogenizing vacuum emulsifiers and automated precision serum filling lines equipped with nitrogen flush systems, we prevent premature oxidation of light-sensitive brightening molecules during bulk containment.
Beaza doesn't rely on off-the-shelf basic bases. Our proprietary joint development framework combines raw-material bioscience, dermatological cell evaluations, clinical patch testing, and multi-tier formulation adjustments. This yields face whitening serums with proven transdermal bio-availability that deliver perceptible pigment dispersion within 14 to 28 days.
Modern consumers demand safe, non-cytotoxic, hydroquinone-free brightening. Our ODM laboratory designs formulas addressing all four critical phases of the pigmentation biological pathway.
Historical face whitening frequently relied on aggressive caustic stripping or toxic tyrosinase inactivation via mercury salts and hydroquinone—both strictly banned by the EU Cosmetic Regulation (EC 1223/2009) and the US FDA. Our cutting-edge private label whitening serums employ biomimetic cell-signaling compounds that safely downregulate endothelin-1, inhibit tyrosinase glycosylation, obstruct melanosome transfer, and accelerate desquamation without damaging epidermal melanocytes.
Blocks UV-induced inflammation cascades. We incorporate high-purity Tranexamic Acid and Glabridin to attenuate plasminogen activation and decrease keratinocyte arachidonic acid liberation, stopping melanin triggers at the origin.
Direct active-site competitive blocking using stabilized Alpha-Arbutin and Liposomal Resveratrol. These actives dock within the copper active center of the enzyme, stopping L-DOPA oxidation without inducing cellular toxicity.
Ultra-pure Niacinamide (cosmetic grade with nicotinic acid under 20ppm to eliminate vasodilation-induced facial redness) arrests up to 68% of melanosome transfer from melanocytes into surrounding baseline keratinocytes.
Subtle micro-doses of biomimetic Mandelic acid, Gluconolactone (PHA), and biological fermented Papain speed stratum corneum shedding, flushing already-pigmented cells while safeguarding barrier hydration integrity.
A single brightening serum cannot fit all geographical environments. Our cosmetic chemists engineer target viscidity, carrier polarity, and active loadings to conquer diverse climatic conditions and local consumer preferences.
Demands: Extreme tropical humidity, high UV index, acne-prone skin profiles.
Solution: Water-burst, ultra-light oil-free hydro-gel base. Incorporates 3% 3-O-Ethyl Ascorbic Acid, Centella Asiatica, and Tea Tree Hydrosol for combined blemish control and tone enhancement with zero stickiness.
Demands: Arid heat, severe hyperpigmentation, intense outdoor UV radiation.
Solution: Emollient-rich micro-emulsion serum containing dual-phase botanical oils, 5% Niacinamide, high-potency Alpha-Arbutin, and Squalane to restore lipid barriers stripped by constant interior air-conditioning.
Demands: Clean beauty, anti-aging convergence, strict "free-from" lists.
Solution: Fragrance-free, vegan certified formulations pairing Ascorbyl Glucoside (AA2G), Bakuchiol, and multi-molecular weight Hyaluronic Acid targeting post-inflammatory erythema (PIE) and age spots with dermatologist clinical claims.
Demands: High melanin density (Fitzpatrick IV–VI), stubborn post-acne marks.
Solution: Non-irritating tyrosinase modulators without cytotoxic agents that cause rebound hypopigmentation. Employs Kojic Acid Dipalmitate, Licorice Root Extract, and Azelaic Acid derivatives.
Launching a high-efficacy brightening serum requires managing oxidation risks, container migration, regulatory notifications, and supply timelines. Beaza acts as your single accountable partner from formulation chemistry to customs clearance.
Whitening compounds degrade under photon and oxygen exposure. We source and customize high-density amber borosilicate glass droppers, UV-metalized PETG bottles, and dual-chamber airless vacuum dispensers that prevent atmospheric contact, assuring 36 months of active ingredient potency without discoloration.
Never let compliance hold back your product launch. Our in-house regulatory affairs team authors complete Product Information Files (PIF), Cosmetic Product Safety Reports (CPSR), Certificate of Free Sale (CFS), and handles direct portal filings across EU CPNP, UK SCPN, US FDA MoCRA, and Saudi SFDA/SASO.
We deliver benchmark lab counter-samples within 3 to 5 business days. Approved pilot batches undergo rigorous multi-temperature accelerated aging checks (4°C, 25°C, 48°C, and 50°C cycle thermal shock for 90 days), centrifuge phase separation testing, and preservative challenge assays (ISO 11930) prior to commercial runs.
Whether you represent a fast-scaling direct-to-consumer digital brand, a supermarket private-label division, or an international luxury dermatology group, our operational model conforms precisely to your purchasing governance criteria.
For cross-border Amazon, TikTok Shop, and Shopify beauty operators, speed to market is paramount. Leverage our 3,500+ proven, safety-tested whitening stock formulas. Choose in-stock componentry with customized UV screen printing for minimum runs starting at just 1,000 units, with turnarounds within 15 working days.
High-volume brands require absolute batch-to-batch homogeneity and full transparency. We provide HPLC assay chromatography for active ingredients, heavy metal ICP-MS quantification (Pb, As, Hg, Cd below 0.1ppm), and total plate count bio-burden records verifying zero pathogen contamination before container departure.
Corporate procurement mandates ethical transparency. Our manufacturing facilities are fully audited and accredited under the Business Social Compliance Initiative (BSCI) and SEDEX (SMETA), guaranteeing fair labor standards, non-animal tested cruelty-free manufacturing, and eco-conscious wastewater filtration systems.
Get straight, clear answers on formulations, shelf stability, production lead times, and international regulatory support directly from our technical manufacturing team.
OEM (Original Equipment Manufacturer) requires you to supply the definitive formulation, active ingredient ratios, and manufacturing protocols. Beaza then carries out compounding, emulsification, and bottling strictly to your blueprint. In contrast, ODM (Original Design Manufacturer) provides a complete, turnkey development solution: our R&D chemists formulate from scratch or tailor one of our 3,500+ clinically verified brightening formulas to match your target claims, packaging aesthetics, texture specifications, and geographic regulatory laws.
We employ a triple-barrier stability system: 1) Chemical stabilization: We utilize advanced Vitamin C derivatives like 3-O-Ethyl Ascorbic Acid and Ascorbyl Glucoside, or chelate pure L-Ascorbic Acid with Ferulic Acid and Tocopherol at an optimized acidic pH of 3.2–3.5. 2) Manufacturing controls: Vacuum emulsification with inert nitrogen gas flushing purges dissolved oxygen from the bulk during mixing and filling. 3) Primary packaging protection: We pair formulas with pharmaceutical-grade UV-coated amber glass, opaque ceramic coatings, or airless pump delivery mechanisms.
For stock private label formulations utilizing standard in-house bottles and droppers, our MOQ starts at 1,000 units. For fully customized chemical formulation development (bespoke viscosity, unique botanical scent profiles, and active percentage adjustments) paired with custom-molded or custom-coated packaging, the standard production threshold is typically 3,000 to 5,000 units, dictated primarily by automated filling line calibration economics.
Every batch leaving our Guangzhou production facilities is supported by a comprehensive batch Certificate of Analysis (COA) and a detailed Safety Data Sheet (SDS/MSDS) formatted to UN GHS standards. Furthermore, we provide GMPC and ISO 22716 factory certificates, Certificates of Free Sale (CFS), qualitative/quantitative INCI disclosures, and full technical documentation necessary to support your local agents in submitting EU CPNP notifications, US FDA MoCRA registrations, or Middle East SASO/SFDA filings.
Yes. Over 65% of our private label brightening serum export portfolio is engineered specifically to meet strict clean-beauty parameters. We formulate without parabens, phthalates, synthetic artificial dyes, mineral oil, formaldehyde releasers, or synthetic fragrances. We source plant-derived solvents, natural bio-ferment gums (such as Sclerotium and Xanthan gum), and vegan hyaluronic acids produced through Streptococcus zooepidemicus bio-fermentation.
Following initial brief consultation, lab counter-samples for texture and fragrance evaluation are dispatched within 3 to 5 business days. Once formulation, component artwork, and primary packaging are formally approved, commercial production generally takes 20 to 25 calendar days. Subsequent re-orders with approved packaging in stock can be produced, filled, and inspected within 10 to 14 business days, followed by sea, air, or rail shipping arrangements.
We perform multi-step laboratory testing before any formulation enters commercial production. In vitro tests verify tyrosinase enzyme inhibition rates. Repeat Insult Patch Testing (RIPT) on human volunteers checks for skin irritation and sensitization. In addition, we execute automated UV accelerated stability audits, heavy metal assay testing via ICP-MS, and standard 28-day preservative challenge tests (ISO 11930) to verify cosmetic longevity and microbiological purity.
Yes, we warmly welcome brand owners, procurement managers, and quality assurance auditors to visit our two manufacturing plants: Guangzhou Aoyan Cosmetics Co., Ltd. and Guangzhou Xinzimei Cosmetics Co., Ltd. We provide full facility walkthroughs across our automated cleanrooms, R&D formulation laboratories, and analytical testing centers. For international buyers unable to travel, we offer live digital video audits and comprehensive third-party inspection access.
A successful beauty brand thrives on synergistic product layering. Expand your retail offerings beyond facial serums with these complementary body, cleansing, and targeted specialty formulations manufactured in our facilities.
