Label: CLEN GERM KILLER-SPRAY- titanium dioxide, hypochlorous acid liquid

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated July 15, 2020

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  • ACTIVE INGREDIENT

    titanium dioxide, hypochlorous acid

  • INACTIVE INGREDIENT

    Coumarin, Linalool, Quercetin, Water

  • PURPOSE

    • Do not dilute spray
    • Use at strength for maximum effectiveness
    • Spray directly, from a distance of about 8 to 10 inches. For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    • Wipe with gauze or cotton swab and let air dry. Spray clothes, equipment, and indoor objects for sterilization and deodorization as required.
  • WARNINGS

    For external use only. 

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

    Stop use and ask a doctor if irritation or rash occurs develop and persist for more than 72 hours.

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

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLEN GERM KILLER-SPRAY 
    titanium dioxide, hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.005 g  in 50 mL
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.004 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    COUMARIN (UNII: A4VZ22K1WT)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    QUERCETIN (UNII: 9IKM0I5T1E)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71544-0005-150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/15/2020
    Labeler - MY Corp.,Ltd (688202781)
    Registrant - MY Corp.,Ltd (688202781)
    Establishment
    NameAddressID/FEIBusiness Operations
    MY Corp.,Ltd688202781manufacture(71544-0005) , label(71544-0005) , pack(71544-0005)
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