We are a one-stop supply chain and manufacturing powerhouse specializing in cosmetics, medical aesthetic products, skincare lines, facial masks, and moisturizing formulations, offering end-to-end OEM and ODM solutions tailored exclusively for cosmetics and medical aesthetic brand partners.
Rooted in a fully integrated supply chain network, we streamline every link from premium raw material sourcing to finished product delivery. Our raw material procurement team partners with globally certified suppliers, ensuring that ingredients for moisturizing serums, medical-grade post-procedure masks, and functional skincare items meet international safety and efficacy standards—including compliance with EU Cosmetics Regulation, FDA guidelines, and regional medical device requirements for aesthetic products. We leverage bulk sourcing advantages to secure cost-effective yet high-quality materials, passing on tangible value to our brand clients without compromising on product integrity.
Our manufacturing facilities boast GMP-certified production lines, equipped with advanced automated mixing, filling, and packaging technologies. We excel in flexible production runs, accommodating both small-batch custom ODM projects and large-scale OEM orders to match brands’ diverse launch and scaling needs. For medical aesthetic products, our dedicated clean workshops adhere to strict sterile production protocols, ideal for crafting sensitive-skin-friendly repair masks, soothing moisturizers, and post-treatment skincare essentials that align with medical aesthetic clinic standards. For daily cosmetics and skincare, we cover a full spectrum of formulations—from hydrating sheet masks and lightweight moisturizers to anti-aging serums—with customizable textures, scents, and active ingredient concentrations to fit distinct brand positioning.
Beyond manufacturing, our in-house R&D center is staffed by a team of chemists, dermatologists, and formulation specialists who stay ahead of global beauty trends and ingredient innovations. We offer comprehensive ODM support: from conceptualizing unique product ideas, conducting market viability assessments, and developing proprietary formulas, to designing eye-catching packaging and preparing full compliance documentation. For OEM collaborations, we ensure precise replication of brand-approved formulas, with rigorous quality control checks at every production stage—raw material inspection, in-process testing, and finished product stability analysis—to guarantee consistency across every batch.
We understand that speed-to-market is critical for brand success. Our optimized supply chain and production workflows cut down lead times significantly, while our responsive account management team provides real-time updates on order progress, raw material availability, and regulatory changes. We also offer value-added services such as packaging sourcing, logistics coordination, and post-delivery technical support, ensuring a seamless, hassle-free partnership from product ideation to shelf launch.
With a proven track record of partnering with emerging DTC beauty brands and established medical aesthetic labels worldwide, we have built a reputation for reliability, innovation, and customer-centricity. Whether you are looking to launch a niche medical aesthetic skincare line, expand your existing moisturizing product range, or develop a custom mask collection, we have the supply chain strength and manufacturing expertise to turn your vision into a market-leading reality.
Partner with us to unlock the full potential of your cosmetics and medical aesthetic brand—where supply chain efficiency meets premium product quality. Contact our business development team today to discuss your custom OEM/ODM requirements.
What is Skincare Product OEM?
Skincare product OEM (Original Equipment Manufacturing) refers to the process where companies outsource the production of their skincare products to professional manufacturing facilities. These facilities handle everything—from sourcing raw materials, formulation design, manufacturing, to packaging—allowing companies to focus on brand management and marketing. This approach helps reduce production costs, enhance efficiency, and ensure product quality.
How to Choose the Right Skincare Product Manufacturer?
When selecting a suitable skincare product manufacturer, consider the following aspects:
Professional Qualifications and Certifications: Verify if the manufacturer possesses necessary production qualifications and certifications, such as GMP (Good Manufacturing Practice) certification.
R&D Capabilities: Understand the manufacturer’s research and development team and capabilities to ensure they can meet your product innovation needs.
Production Equipment and Technology: Review the manufacturer’s equipment and technological level to ensure they can provide consistent product quality.
Quality Control: Learn about the manufacturer’s quality control processes and standards to ensure products meet market demands and legal regulations.
Reputation and Case Studies: Check client reviews and the manufacturer’s successful cases to gauge their industry reputation and experience.
How is the Cost of Skincare Product OEM Calculated?
The cost of skincare product OEM typically includes the following components:
Raw Material Costs: The cost of active ingredients, auxiliary materials, fragrances, colorants, etc.
Formulation Development Costs: Fees for the manufacturer to develop specific formulations for clients.
Production Costs: This covers labor, machinery, equipment usage, and energy consumption during the manufacturing process.
Packaging Costs: Costs associated with packaging materials, design, and the packaging process.
Testing and Certification Fees: Fees for quality assurance and compliance testing and certification to ensure product quality and legal compliance.
Logistics Costs: Transportation fees from the manufacturer to the client’s specified location.
The actual cost varies depending on product complexity, production scale, and the manufacturer’s pricing standards. A detailed discussion and contract with the manufacturer can ensure transparency and cost control.
What are the Benefits of Skincare Product OEM?
Skincare product OEM offers several advantages, including:
Cost Reduction: Companies can save on the high costs associated with building factories, purchasing equipment, and hiring technical staff, allowing them to allocate resources toward marketing and brand building.
Increased Efficiency: Professional manufacturers have well-established production lines and technology, enabling fast, large-scale production and shortening time-to-market.
Guaranteed Quality: Manufacturers often possess advanced quality control systems and certifications, ensuring products meet high-quality standards.
Focus on Core Business: Companies can concentrate on brand management, product design, and marketing, without diverting attention to production management.
By choosing a reliable partner, businesses can streamline their operations and deliver high-quality skincare products more efficiently.
The following is a checklist of core compliance certifications/registrations for cosmetics in the Americas, Europe, the UK, Japan, South Korea, Southeast Asia, Australia and New Zealand. It covers key markets for cosmetics export, with mandatory items and applicable product categories clearly indicated for quick reference.
I. Americas
1. United States
FDA Enterprise Registration + Product Listing (Mandatory starting from MoCRA 2025): Processed via the VCRP system and updated every 2 years; overseas enterprises must appoint a US agent; applicable to all cosmetics.
Label Compliance (Mandatory): Ingredients labeled in INCI nomenclature, net content specified, and all information in English, complying with 21 CFR 701; OTC products such as sunscreens shall be declared as pharmaceuticals.
CPSR Report: Non-mandatory, but often required by importers/platforms to prove ingredient safety.
TSCA Compliance: Products containing specific chemical substances need to be registered with the EPA; applicable to cosmetics with preservatives/fragrances.
2. Canada
CND Cosmetic Notification (Mandatory): Required by Health Canada, to be submitted within 10 days after product launch; labels must be bilingual (English-French).
NPN Number (Mandatory for health products): Required for natural health products, not applicable to cosmetics.
3. Mexico
COFEPRIS Registration (Mandatory): Administered by the Federal Commission for the Protection against Sanitary Risks. Imported cosmetics require enterprise registration plus product registration, complying with ingredient and labeling requirements.
4. South America
ANVISA Registration (Mandatory, Brazil): Administered by the National Health Surveillance Agency. Cosmetics need to be registered/filed, with ingredient safety data provided and labels in Portuguese.
ANMAT Registration (Mandatory, Argentina): Administered by the National Administration of Drugs, Food and Medical Technology. Registration is required for imported cosmetics to meet safety and labeling standards.
ISP Registration (Mandatory, Chile): Administered by the Institute of Public Health. Cosmetic enterprises need to complete registration plus product filing, satisfying ingredient and labeling requirements.
II. Europe & The UK
1. EU 27 Member States
◦ CPNP Notification (Mandatory): To be notified via the system before product launch, with CPSR and EU Responsible Person (RP) information submitted; valid across the entire EU territory.
CPSR Report (Mandatory): Compiled by EU-registered cosmetic safety experts, including ingredient assessment and toxicological data.
Appointment of EU Responsible Person (RP) (Mandatory): Non-EU enterprises must appoint an RP who is responsible for compliance and product recalls.
Label Compliance (Mandatory): Ingredients labeled in INCI nomenclature, PAO shelf life indicated, RP information included, and all content in an official EU language.
REACH Compliance: Raw materials must meet restriction requirements; substances of very high concern (SVHC) need to be notified.
2. The United Kingdom
UKCPNP Notification (Mandatory): An independent system established after Brexit, with procedures similar to CPNP; a UK Responsible Person must be appointed.
CPSR Report (Mandatory): Compiled by UK-recognized experts or EU reports recognized by UK authorities.
Northern Ireland: Enterprises can choose either CPNP or UKCPNP for notification, and the responsible person can be an entity established in the EU or the UK.
III. Japan & South Korea
1. Japan
MHLW Registration (Mandatory): Includes manufacturer/distributor registration plus product declaration, categorized into cosmetics and quasi-drugs (e.g., sunscreens, whitening products).
Label Compliance (Mandatory): Ingredients, efficacy and usage precautions must be labeled in Japanese.
Quasi-drug Registration (Mandatory): Products such as sunscreens and freckle-removing cosmetics require clinical trials and approval through the pharmaceutical registration pathway.
2. South Korea
MFDS SCPN Notification (Mandatory for ordinary cosmetics): A safety notification system replacing the former KFDA registration.
Functional Cosmetics Registration (Mandatory): Anti-wrinkle, whitening and other functional products require clinical trials and approval by the MFDS.
KC Safety Test (Mandatory): Products must pass safety tests, and labels must be in Korean.
IV. Southeast Asia (ASEAN)
• Core Rules: Comply with the ASEAN Cosmetics Directive (ACD), with ingredient standards referencing the EU; implementation details vary by country.
• ACIM System Registration (Recommended): ASEAN Cosmetics Information Management System, mandatory in some member states.
• Country-specific Requirements:
BPOM Registration (Mandatory, Indonesia): Administered by the National Agency of Drug and Food Control. Registration is required for imported cosmetics, with CPSR provided.
FDA Registration (Mandatory, Thailand): Administered by the Food and Drug Administration. Requires enterprise registration plus product notification.
NPRA Registration (Mandatory, Malaysia): Administered by the National Pharmaceutical Regulatory Agency. Cosmetic notification is required to meet ACD ingredient requirements.
HSA Registration (Mandatory, Singapore): Administered by the Health Sciences Authority. Registration is required for imported cosmetics, with labels in English.
V. Australia & New Zealand
1. Australia
TGA Registration (for ordinary cosmetics): Administered by the Therapeutic Goods Administration. Ordinary cosmetics require notification; products such as sunscreens shall be registered as pharmaceuticals.
Label Compliance (Mandatory): Ingredients, net content and usage instructions in English; evidence must be provided to support efficacy claims.
2. New Zealand
MPI Registration (Mandatory): Administered by the Ministry for Primary Industries. Cosmetic enterprises need to complete registration plus product notification, complying with safety and labeling standards.
ACVM Compliance: Compliance with animal product regulations; cosmetics containing animal-derived ingredients require additional approval.
Supplementary Notes
1. MSDS/SDS: Globally accepted safety data sheet for chemicals, essential for cross-border transportation and customs clearance.
2. Voluntary Certifications: Such as USDA Organic and ISO22716 GMP, which can enhance market recognition but are not mandatory for market access.