Label: VAXOL PURI- phenoxyethanol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 November 17, 2021

If you are a consumer or patient please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!