Label: HY-IQ HAND AND SURFACE DISINFECTANT AND SANITIZER- hy-iq water spray

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

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Drug Label Information

Updated July 15, 2021

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  • ACTIVE INGREDIENT

    Hy- IQ Water ( [H9O4] | [H5O2] )

    Hydrogen Cation .77%

  • PURPOSE

    Antimicrobial

  • INDICATIONS & USAGE

    For spraying on hands or hard surfaces in order to prevent the spreading of bacteria & harmful germs.

  • WARNINGS

    For External use only. Do not use if you are allergic to any ingredients. Stop use if a rash develops and ask a doctor right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • DOSAGE & ADMINISTRATION

    Spray liberally on hard surfaces or hands. Allow to either dry naturally by air, or by drying with a clean paper towel, fabric towel or sponge

  • OTHER SAFETY INFORMATION

    Store under 110°F (43C)

  • INACTIVE INGREDIENT

    Water, UREA

  • Hy-IQ HAND and SURFACE DISINFECTANT AND SANITIZER

    Hy-IQ HAND and SURFACE DISINFECTANT AND SANITIZER Hy-IQ Hand & surface Disinfectant & Sanitizer

  • INGREDIENTS AND APPEARANCE
    HY-IQ HAND AND SURFACE DISINFECTANT AND SANITIZER 
    hy-iq water spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76701-362
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN CATION (UNII: 5046UKT60S) (HYDROGEN CATION - UNII:5046UKT60S) HYDROGEN CATION10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 940 mg  in 1 mL
    UREA (UNII: 8W8T17847W) 50 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76701-362-16473.176 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2021
    2NDC:76701-362-0250.275 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2021
    3NDC:76701-362-32946.353 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2021
    4NDC:76701-362-763785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/17/2021
    Labeler - HAND SANITIZER LLC (117473019)
    Establishment
    NameAddressID/FEIBusiness Operations
    HAND SANITIZER LLC117473019label(76701-362) , pack(76701-362) , manufacture(76701-362)
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