Label: ABSOCLEAN-S SANITIZING MIST- hypochlorous acid liquid

  • NDC Code(s): 75644-002-01, 75644-002-02, 75644-002-03
  • Packager: KEWS CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 January 18, 2022

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  • ACTIVE INGREDIENT

    HYPOCHLOROUS ACID -- 0.006%

  • Inactive Ingredients

    Water

  • Purpose

    Antimicrobial

  • Directions for Use

    -Use when soap and water not available to supplement regular hand washing.

    -Apply liberally to hands and rub hands thorougly until product is dried

    -Spray enough to the suspected tool, furniture and space.

  • Intended Use

    -For personal sanitizing to decrease bacteria on skin

    -Recommended for repeated use

  • Purpose

    -For personal sanitzing to decrease bacteria on skin

    -Recommended for repeated use

  • Warnings

    For External Use

  • 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.

  • 100mL PDP

    100mL NDC 75644-002-01 ABSOCLEAN-S-100ml

  • 500mL PDP

    500mL NDC 75644-002-02 AbsoClean-S 500mL

  • 20LT PDP

    20LT NDC 75644-002-03 Absoclean-S 20LT

  • INGREDIENTS AND APPEARANCE
    ABSOCLEAN-S SANITIZING MIST 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.006 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75644-002-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/30/2020
    2NDC:75644-002-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/30/2020
    3NDC:75644-002-0320000 mL in 1 JUG; Type 0: Not a Combination Product04/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/30/2020
    Labeler - KEWS CORPORATION (688640317)
    Registrant - KEWS CORPORATION (688640317)
    Establishment
    NameAddressID/FEIBusiness Operations
    KEWS CORPORATION688640317manufacture(75644-002) , pack(75644-002) , label(75644-002)