China Wholesale Skincare Products Factories & Contract Manufacturing Hub

Under the Modernization of Cosmetics Regulation Act (MoCRA), our manufacturing facilities maintain active FDA Cosmetic Facility Registrations with established FEI numbers. We supply complete Ingredient Disclosure dossiers, quantitative fragrance allergen declarations, certified testing records for USP 51 preservative efficacy (challenge testing), safety substantiation records, and professional toxicological assessments. Our regulatory team also prepares technical dossiers for electronic product listing via the FDA Cosmetics Direct portal on behalf of our brand partners.

We provide a tiered MOQ structure designed to support both agile venture launches and high-volume multinational programs. For standardized, ready-to-label active formulas utilizing in-stock standardized packaging, MOQs start as low as 500 to 1,000 units per SKU. For fully bespoke custom formulations requiring unique chemical research, targeted active concentrations, custom fragrance profiles, or customized molded packaging components, standard production runs typically start at 3,000 to 5,000 units. Bulk liquid, cream, or scrub shipments in 200L drums or 5-gallon containers start at 100 kg.

Intellectual property parameters are explicitly governed by clear contract manufacturing agreements. When a client commissions a completely custom formulation through paid R&D fees, the resulting proprietary chemical formulation matrix and master batch record become the client's sole IP upon fulfillment of contract volume milestones. Alternatively, clients selecting our proven white-label base formulas receive an exclusive, royalty-free commercial market license for their designated brand name and sales territory.

Every manufactured production batch is tested against a rigorous five-tier analytical matrix. This encompasses: (1) Organoleptic and physical properties (appearance, odor, color, spindle Brookfield viscosity, dynamic pH at 25°C, specific gravity); (2) Phase separation centrifuge testing at 3,500 RPM for 30 minutes; (3) Heavy metal testing via Inductively Coupled Plasma Mass Spectrometry (ICP-MS) ensuring Lead (<2ppm), Arsenic (<1ppm), Mercury (<0.1ppm), and Cadmium (<1ppm); (4) Total Aerobic Microbial Count (TAMC <100 CFU/g) and Total Yeast/Mold Count (TYMC <10 CFU/g) with absolute absence of Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans; (5) High-Performance Liquid Chromatography (HPLC) to verify active ingredient concentration claims.

Standard prototype lab formulation samples are typically dispatched within 7 to 10 business days from receipt of a finalized product brief. Client sensory revisions take approximately 5 to 7 business days per cycle. Once pre-production samples and packaging artwork are approved, commercial bulk manufacturing and filling require 25 to 35 business days, depending on packaging component complexity (e.g., custom color injection, electroplating, or hot-stamping). Repeat replenishment orders are typically fulfilled in 15 to 20 business days.

Yes. For distribution within the European Economic Area (EEA) and the United Kingdom under Regulation (EC) No 1223/2009, we compile comprehensive Product Information Files (PIF). We partner directly with certified Eurofins and SGS toxicologists to execute the Cosmetic Product Safety Report (CPSR Part A and Part B), stability testing, packaging interaction validation, and complete technical notification onto the European Cosmetic Product Notification Portal (CPNP).

We support all standard Incoterms 2020: EXW (Ex Works), FOB (Free on Board - Shenzhen, Guangzhou, Ningbo, or Shanghai ports), CIF (Cost, Insurance, and Freight), and complete DDP (Delivered Duty Paid) door-to-door freight. Under DDP terms, our supply chain division coordinates maritime ocean freight, customs declarations, import tariff clearance, destination port drayage, and scheduled appointment deliveries into regional 3PL networks or Amazon FBA fulfillment centers across North America, Europe, Oceania, and the GCC.

China has officially eliminated mandatory pre-market and post-market animal testing for all qualifying imported and domestic "ordinary cosmetics" (including moisturizers, cleansers, serums, lipsticks, and shampoos) that hold ISO 22716 or GMP quality certifications. Our complete manufacturing lines operate under strict cruelty-free protocols. We require non-animal testing declarations from all tier-1 upstream botanical and chemical raw material suppliers, enabling our clients to achieve and maintain Leaping Bunny, Cruelty-Free International, and PETA certifications with full audit documentation.