Label: MELAO TATTOO BUTTER- tocopheryl acetate jelly

  • NDC Code(s): 83566-110-01
  • Packager: Guangzhou Yilong Cosmetics Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 20, 2024

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  • ACTIVE INGREDIENT

    .ALPHA.-TOCOPHEROL ACETATE, DL-

  • PURPOSE

    Lubricates & Moisturizes

  • INDICATIONS & USAGE

    Use as needed to help maintain your tattoo's crispness and promote it'slongevity.

  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • DO NOT USE

    Do not use on damaged or broken skin.

  • WHEN USING

    When using this product keep out of eyes. Rinse with water to remove.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Take a dime-sized amount and apply it to the tattoo area.

  • INACTIVE INGREDIENT

    SIMMONDSIA CHINENSIS SEED
    SUNFLOWER SEED
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES
    MACADAMIA TERNIFOLIA WHOLE
    SYNTHETIC BEESWAX

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MELAO TATTOO BUTTER 
    tocopheryl acetate jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU) (BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES - UNII:0C9AC7D6XU) BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES56.74 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SUNFLOWER SEED (UNII: R9N3379M4Z)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)  
    MACADAMIA TERNIFOLIA WHOLE (UNII: 480C47LI24)  
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-110-01150 g in 1 BOX; Type 0: Not a Combination Product03/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/09/2024
    Labeler - Guangzhou Yilong Cosmetics Co., Ltd (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co., Ltd712647107manufacture(83566-110)
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