Label: DR.VIR GERM PEROXYACETIC ACID MULTI-DISINFECTANT- peroxyacetic acid liquid

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

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Drug Label Information

Updated July 21, 2020

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  • ACTIVE INGREDIENT

    alcohol, Peroxyacetic acid

  • INACTIVE INGREDIENT

    Water, Surfactants : Polyoxyethylene alkyl ether (nonionic)

  • PURPOSE

    multi disinfectant

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    1. Sprinkle 20 cm away until moist 2.It is more effective if sprayed repeatedly every day.[Storage precautions] Store at room temperature(1-30 degrees Celsius) [labeling items of household chemicals subject to safety verification]

  • WARNINGS

    1. When it gets into your eyes, do not rub them, immediately wash them with clean water, and if there is any abnormality, consult a doctor.

    2. Do not drink it, or if you drink it, take measures such as drinking water or milk, and

    then consult a doctor.

    3. Do not use for any purpose other than

    4. Do not spray directly on humans or food

    5. Do not mix with other products.

    6. Do not place in direct sunlight or in high temperature.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DR.VIR GERM PEROXYACETIC ACID MULTI-DISINFECTANT 
    peroxyacetic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69255-800
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERACETIC ACID (UNII: I6KPI2E1HD) (PERACETIC ACID - UNII:I6KPI2E1HD) PERACETIC ACID5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PAEONIA LACTIFLORA ROOT OIL (UNII: BC82X683T4)  
    WATER (UNII: 059QF0KO0R)  
    CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69255-800-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/26/2020
    Labeler - JANGIN PHARM CO.,LTD. (688733680)
    Registrant - JANGIN PHARM CO.,LTD. (688733680)
    Establishment
    NameAddressID/FEIBusiness Operations
    JANGIN PHARM CO.,LTD.688733680manufacture(69255-800)
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