Label: VIRUS ZERO-F- chlorine dioxide liquid

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

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Drug Label Information

Updated August 13, 2020

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  • Active ingredient

    chlorine dioxide 0.02%

  • Purpose

    Antiseptic

  • Use

    Medical facilities, schools, and businesses, group catering facilities, food service facilities sterilization, furniture, refrigerators, toilets

  • Warnings

    Do not use other than the purpose of the product / Keep in a cool place away from direct sunlight

    in children less than 2 months of age / on open skin wounds

  • When using this product

    Vomit when drinking contents and consult your doctor / Rinse immediately when eye contact occurs

  • Stop use and ask a doctor

    if irritation or rash occurs. These may be signs of a serious condition.

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Turn the spray nozzle to fit on / Sprinkle at a distance / when sprayed in large quantities wipe lightly with a dry towel / Sufficient ventilation required for use in confined spaces

    • Supervise children under 6 year of age when using this product to avoid swallowing.

  • Other information

    • Store between 12-30C (59-86F)

    • Avoid freezing and excessive heat above 40C (104F)

  • Inactive ingredient

    water

  • Package Label

    300ml NDC: 90105-201-01 Label

  • INGREDIENTS AND APPEARANCE
    VIRUS ZERO-F 
    chlorine dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90105-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE0.02 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90105-201-01300 mL in 1 BOTTLE; Type 0: Not a Combination Product08/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/14/2020
    Labeler - O2 (695032447)
    Registrant - O2 (695032447)
    Establishment
    NameAddressID/FEIBusiness Operations
    O2695032447manufacture(90105-201)
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