ISLEAF CUSHION CONCEALER 21 (TITANIUM DIOXIDE) LIQUID [C3 CO., LTD.]

ISLEAF CUSHION CONCEALER 21 (TITANIUM DIOXIDE) LIQUID [C3 CO., LTD.]
PDF | XML

NDC 70818-001-01
Set ID 55bf9c1f-9c65-7021-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager C3 Co., Ltd.
Generic Name
Product Class
Product Number
Application Number PART347
  • ACTIVE INGREDIENT

    titanium dioxide

  • INACTIVE INGREDIENT

    wter butylene glycol, beeswas, etc.

  • PURPOSE

    brighten around eyes or face

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Click end to release product into brush, then apply to areas you want to perfect and brighten around eyes or face. Repeat until desired coverage is achieved, then pat into skin with fingertips to blend flawlessly.

  • WARNINGS

    1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
    1) Occurrence of red spots, swelling, itchiness, and other skin irritation
    2) If the symptoms above occur after the application area is exposed to direct sunlight
    2. Do not use on open wounds, eczema, and other skin irritations
    3. Precaution for Storage and Handling
    1) Close the lid after use
    2) Keep out of reach of infants and children
    3) Do not to store in a place with high/low temperature and exposed to direct sunlight

    4. Use as avoiding eye areas.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ISLEAF CUSHION CONCEALER 21 
    titanium dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70818-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1.6 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70818-001-013.5 g in 1 APPLICATOR; Type 0: Not a Combination Product08/08/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34708/08/2017
    Labeler - C3 Co., Ltd. (689846633)
    Registrant - C3 Co., Ltd. (689846633)
    Establishment
    NameAddressID/FEIBusiness Operations
    C3 Co., Ltd.689846633manufacture(70818-001) , label(70818-001) , pack(70818-001)

Related Drugs