Label: HUUREKA SANITIZER- hypochlorous acid liquid

  • NDC Code(s): 75644-001-01, 75644-001-02, 75644-001-03, 75644-001-04, view more
    75644-001-05, 75644-001-06
  • 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 ------ 0.0.007%

  • Purpose

    Antimicrobial

  • Directions for Use:

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

    Apply liberally to hands and rub hands thoroughly until product is dried.

    Spray enough to the suspected tool, furniture and space.

  • Inactive Ingredient(s)

    Water

  • Intended Use

    For Personal sanitizing to decrease baceteria on skin

    Recommended for repeated use.

  • Warnings:

    For External Use

  • Purpose:

    For personal sanitizing to decrease bacteria on skin.

    Recommened 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.

  • 100 mL PDP

    100mL NDC 75644-001-001 HUUREKA 100mL PDP

  • 500 mL PDP

    500 mL NDC 75644-001-002 HUUREKA 500mL PDP

  • 2 LT PDP

    2 LT PDP 75644-001-04

    HUUREKA 2LT PDP

  • 4 LT PDP

    4 LT PDP, NDC: 75644-001-05

    Huureka 4LT PDP

  • 10 LT PDP

    10 LT PDP, NDC 75644-001-06

    Huureka 10L PDP

  • 20LT PDP

    20 LT NDC 75644-001-003 Huureka 20LT PDP

  • INGREDIENTS AND APPEARANCE
    HUUREKA SANITIZER 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-001
    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:75644-001-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
    2NDC:75644-001-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
    3NDC:75644-001-0320000 mL in 1 JUG; Type 0: Not a Combination Product05/01/2020
    4NDC:75644-001-042000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
    5NDC:75644-001-054000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
    6NDC:75644-001-0610000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2020
    Labeler - KEWS CORPORATION (688640317)
    Registrant - KEWS CORPORATION (688640317)
    Establishment
    NameAddressID/FEIBusiness Operations
    KEWS CORPORATION688640317pack(75644-001) , manufacture(75644-001) , label(75644-001)
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