Label: BELSON ALCOHOL FREE HAND SANIZITER- hypochlorous acid liquid

  • NDC Code(s): 75644-003-01, 75644-003-02, 75644-003-03, 75644-003-04, view more
    75644-003-05
  • Packager: KEWS CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 18, 2022

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  • ACTIVE INGREDIENT

    HYPOCHLOROUS ACID -- 0.007%

  • 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

  • USES

    -For personal sanitzing to decrease bacteria on skin

    -Recommended for repeated 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.

  • Warnings

    For External Use

  • 100mL PDP

    BELSON 100mL PDP100mL NDC 75644-003-01

  • 500mL PDP

    BELSON 500ML PDP500mL NDC 75644-003-02

  • 1LT PDP

    1LT NDC 75644-003-03 BELSON 1LT PDP

  • 4LT PDP

    4LT NDC 75644-003-04 BELSON 4L PDP

  • 20LT PDP

    BELSON 20LT PDP20LT NDC 75644-003-05

  • INGREDIENTS AND APPEARANCE
    BELSON ALCOHOL FREE HAND SANIZITER 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.007 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75644-003-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/19/2020
    2NDC:75644-003-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/19/2020
    3NDC:75644-003-031000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
    4NDC:75644-003-044000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
    5NDC:75644-003-0520000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/19/2020
    Labeler - KEWS CORPORATION (688640317)
    Registrant - KEWS CORPORATION (688640317)
    Establishment
    NameAddressID/FEIBusiness Operations
    KEWS CORPORATION688640317manufacture(75644-003) , pack(75644-003) , label(75644-003)
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