Label: CLOH LIVING HAND SANITIZER- hypochlorous acid spray

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated June 17, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!