Label: GZE EUCALYPTUS OIL- eucalyptus globulus leaf oil oil

  • NDC Code(s): 83566-132-01
  • Packager: Guangzhou Yilong Cosmetics Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 17, 2024

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  • ACTIVE INGREDIENT

    Eucalyptus Globulus Leaf Oil

  • PURPOSE

    GZE eucalyptus oil carimprove scalp conditinand makes hair look more shiny. lt can also make skin more hydrated and smooth.

  • INDICATIONS & USAGE

    For hair, squeeze some eucalyptus oil on your hands and mix well,then apply to your hair and massage into your scalp to absorb.For skin, apply a small amount of eucalyptus oil to the palm, gently rub to warm and apply to face.

  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • DO NOT USE

  • 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

    For hair, squeeze some eucalyptus oil on your hands and mix well,then apply to your hair and massage into your scalp to absorb.For skin, apply a small amount of eucalyptus oil to the palm, gently rub to warm and apply to face.

  • INACTIVE INGREDIENT

    water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    GZE EUCALYPTUS OIL 
    eucalyptus globulus leaf oil oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-132
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF100 g  in 118 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-132-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/22/2023
    Labeler - Guangzhou Yilong Cosmetics Co., Ltd (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co., Ltd712647107manufacture(83566-132)
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