Label: CLOH LIVING HAND SANITIZER- hypochlorous acid spray

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

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Drug Label Information

Updated June 17, 2022

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  • Active Ingredient(s)

    Hypochlorous Acid 0.0035%. Purpose: Antimicrobial

  • Purpose

    Antimicrobial, Hand Sanitizer

  • Use

    Hand sanitizer to help reduce bacteria on the skin.
    Recommended for repeated use.

  • Warnings

    For external use only-hand.

  • Do not use

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

  • 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

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Other information

    • Store at room temperature 1oC-30oC ( 33.8oF-86oF).
  • Inactive ingredients

    Purified Water.

  • Package Label - Principal Display Panel

    CLOH Living Hand Sanitizer Spray

  • INGREDIENTS AND APPEARANCE
    CLOH LIVING HAND SANITIZER 
    hypochlorous acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79617-200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.0035 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79617-200-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2022
    2NDC:79617-200-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2022
    3NDC:79617-200-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/2022
    4NDC:79617-200-044000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/2022
    5NDC:79617-200-0520000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/2022
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/17/2022
    Labeler - SpaceLink Corporation (689464352)
    Registrant - SpaceLink Corporation (695898222)
    Establishment
    NameAddressID/FEIBusiness Operations
    SpaceLink Corporation695898222manufacture(79617-200)
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