Label: CHLORINIE DISINFECTANT liquid

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

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Drug Label Information

Updated April 16, 2020

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  • Active Ingredient(s)

    HYPOCHLOROUS ACID 12%

  • Purpose

    Antiseptic

  • Use

    AIR,HAND,OBJECT SURFACE AND OTHER SCENES.

  • Warnings

    STORED IN A COOL,VENTILATED AND DRY PLACE ,USE THIS PRODUCT AS SOON AS POSSIBLE AFTER OPENING THE BOTTLE.DO NOT DRINK.

  • Do not use

    Not for human body

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    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.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.Not for human body

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Spray the product evenly on the surface of the object or finger to be sterilized,without wiping or cleaning.

  • Other information

    STORED IN A COOL,VENTILATED AND DRY PLACE ,USE THIS PRODUCT AS SOON AS POSSIBLE AFTER OPENING THE BOTTLE.

  • Inactive ingredients

    water

  • Package Label - Principal Display Panel

    500ml

  • INGREDIENTS AND APPEARANCE
    CHLORINIE DISINFECTANT 
    chlorinie disinfectant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75434-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID12 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75434-005-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/16/2020
    Labeler - Fujian Xialu Electrochemical Co., Ltd. (527297457)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fujian Xialu Electrochemical Co., Ltd.527297457manufacture(75434-005)
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