Label: ONTREE LIFE- chlorine dioxide, anatase liquid

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

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Drug Label Information

Updated September 4, 2020

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  • Active ingredient

    Chlorine dioxide 0.02%

    Anatase 0.05%

  • 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

    500ml NDC: 90105-202-01 Label

  • INGREDIENTS AND APPEARANCE
    ONTREE LIFE 
    chlorine dioxide, anatase liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90105-202
    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
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90105-202-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/04/2020
    Labeler - O2 (695032447)
    Registrant - O2 (695032447)
    Establishment
    NameAddressID/FEIBusiness Operations
    O2695032447manufacture(90105-202)
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