Label: VAXOL PURI- phenoxyethanol liquid

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated November 17, 2021

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  • Active Ingredient

    Phenoxyethanol 1.5%

  • Purpose

    Antiseptic

  • Use

    For use on clothing or people, Spray it at home, at school, at the office, Stores and spaces with a large floating population, Target requiring sterilization and deodorization.

  • Warnings

    Check the label before use, Do not throw or drop, People with damaged skin should be careful not to come into contact for a long time, Don't drink.

  • Do not use

    On open skin wounds, Do not drink.

  • When using this product

    If it gets into your eyes Rinse immediately with water.

  • Ask Doctor

    If skin irritation or red spots appear, seek medical treatment. If you eat or swallow, take first aid and consult your doctor immediately.

  • Keep out of reach of children

    Be careful not to put it in your child's mouth.

  • Directions

    Spray on a target that requires sterilization and deodorization, Use for air sterilization in crowded places, Use for children's supplies, toys and clothing, Use in stinking or unsanitary spaces.

  • Inactive ingredient

    Purified Water, Hexanediol, d-Limonene, alpha-Pinene, gamma-Terpinene, para-Cymene

  • Package Label

    50ml VAXOL PURI 81268-201-01

  • INGREDIENTS AND APPEARANCE
    VAXOL PURI 
    phenoxyethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81268-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T) (PHENOXYETHANOL - UNII:HIE492ZZ3T) PHENOXYETHANOL1.5 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .GAMMA.-TERPINENE (UNII: 4YGF4PQP49)  
    WATER (UNII: 059QF0KO0R)  
    P-CYMENE (UNII: 1G1C8T1N7Q)  
    HEXANEDIOL (UNII: ZIA319275I)  
    .ALPHA.-PINENE (UNII: JPF3YI7O34)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81268-201-0150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    2NDC:81268-201-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/17/2020
    3NDC:81268-201-032000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/17/2020
    Labeler - OPENKOREA CO., Ltd (695742727)
    Registrant - OPENKOREA CO., Ltd (695742727)
    Establishment
    NameAddressID/FEIBusiness Operations
    OPENKOREA CO., Ltd695742727manufacture(81268-201)
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