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Cosmetics

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Cosmetics

Related Regulations
  • European Union
    - EU Cosmetic Regulation (EC) No.1223/2009
    - CPNP (Cosmetic Products Notification Portal)
  • United States
    - MoCRA (Modernization of Cosmetics Regulation Act of 2022)
    - FDA Cosmetic Facility & Product Registration
  • United Kingdom
    - UK Cosmetic Regulation
    - SCPN Notification
  • Asia
    - Korea Cosmetic Act (MFDS)
    - China NMPA Cosmetic Regulation (CSAR)
    - ASEAN Cosmetic Directive (ACD)
    - Japan PMD Act (Cosmetics)
  • Others
    - Middle East (GSO / SFDA / UAE ECAS 등)
    - Canada Cosmetic Notification Form (CNF)
    - Australia AICIS Regulation
Target Products
Cosmetic products intended for cleansing, beautifying, perfuming, or enhancing the appearance of the human body.
Skincare Products Skincare products, Lotions and creams, Essences and serums
Color Cosmetics Makeup products, Lip products, Eye makeup products
Hair & Body Care Shampoo and conditioner, Body wash and body lotion, Deodorants
Functional & Special Cosmetics Sunscreen products, Whitening / anti-wrinkle products, Personal care products
Others Fragrances and perfuming products, Children's cosmetics, E-commerce distributed cosmetics
Procedure
  • Product classification and market-specific regulatory review
  • Ingredient (INCI) verification and restricted/prohibited substance review
  • Product safety assessment
  • Establishment of Product Information File (PIF)
  • Appointment of Responsible Person (RP) or local responsible entity
  • Product notification and registration
  • Labeling and claims compliance review
  • Market placement and post-market safety management
Period for acquisition
Approximately 2–8 weeks
(May vary depending on country registration procedures and completeness of submitted documentation.)
Materials required
  • Full ingredient list (INCI List)
  • Formulation information and raw material MSDS
  • Product safety assessment documentation
  • Manufacturing process overview and manufacturing site information
  • GMP or manufacturing quality-related documentation
  • Product testing reports (if applicable)
  • Labeling artwork and regulatory markings
  • Product claims and marketing statements
  • Responsible Person (RP) or local representative information
  • Product photos and packaging information