Label: ISLEAF TATTOO EYEBROW BROWN- methylparaben gel

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated August 8, 2017

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  • ACTIVE INGREDIENT

    methylparaben

  • INACTIVE INGREDIENT

    water, butylene glycol, glycerin, alcohol, xanthan gum, etc

  • PURPOSE

    for a tattoo effect

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Shake the ball inside of the product before use, then press the tip of container and draw eyebrows. In about 5 hours, the eyebrows will look natural.

  • 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 TATTOO EYEBROW BROWN 
    methylparaben gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70818-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYLPARABEN (UNII: A2I8C7HI9T) (METHYLPARABEN - UNII:A2I8C7HI9T) METHYLPARABEN0.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70818-007-012.5 g in 1 APPLICATOR; Type 0: Not a Combination Product08/08/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/08/2017
    Labeler - C3 Co., Ltd. (689846633)
    Registrant - C3 Co., Ltd. (689846633)
    Establishment
    NameAddressID/FEIBusiness Operations
    C3 Co., Ltd.689846633label(70818-007) , pack(70818-007) , manufacture(70818-007)