Label: CHAMPUREGREEN- hypochlorous acid liquid

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated October 20, 2022

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  • Active ingredient[s]

    HOCL(Hypochlorous acid) 0.005%

  • Purpose

    Antiseptic

  • Use[s]

    Helps reduce disease-causing germs and viruses that may exist on objects and in spaces.

  • Warnings

    For external use only

  • Do not use

    • Do not mix with water or other chemicals.
    • Do not spray directly on electric products or electronics.
    • Do not use the product for any other purpose than its intended purpose.
  • Keep out of reach of children

    Keep out of reach of children.

  • Stop use

    • If swallowed, drink enough water. If abnormal symptoms occur, get medical help.
    • Keep out of eyes. In case of contact with eyes, flush thoroughly with clean water. If abnormal symptoms occur, consult a doctor.
    • Stop use if skin irritation or redness develops.
  • Directions

    • Spray from a certain distance on where disinfection is needed.
    • Use frequently when needed.
    • Let it to dry or wipe with a cloth.
  • Other information

    Best before : 6 months after opening

    Expiration date : indicated separately

    Store at room temperature and avoid direct sunlight and high temperatures.

  • Inactive ingredient

    Purified Water

  • Package Label

    81745-501-03

    81745-501-01

    81745-501-02

  • INGREDIENTS AND APPEARANCE
    CHAMPUREGREEN 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81745-501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.005 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81745-501-01300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/10/2021
    2NDC:81745-501-0280 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/10/2021
    3NDC:81745-501-0317 mL in 1 CONTAINER; Type 0: Not a Combination Product09/16/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/10/2021
    Labeler - PROSAFEBIO (695501710)
    Registrant - PROSAFEBIO (695501710)
    Establishment
    NameAddressID/FEIBusiness Operations
    PROSAFEBIO695501710manufacture(81745-501)
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