Label: HY-IQ SURFACE CLEANER- hy-iq water spray

  • 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 June 23, 2021

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  • ACTIVE INGREDIENT

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

    Hydrogen Cation .77%

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    Surface cleaning. Helps prevent the risk and spread of infection and communicable diseases by killing germs that reside on skin and surfaces.

  • 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 your surface throroughly, then wipe until dry. For maximum efficacy, we recommend using with a Hy-IQ® BioFoam™ Mitt, a Hy-IQ® Biofoam™ Sponge, or a Hy-IQ® BioFoam™ Wipe, for an even better clean.

  • OTHER SAFETY INFORMATION

    Store under 110°F (43°C)

  • INACTIVE INGREDIENT

    WATER, UREA

  • PRINCIPAL DISPLAY PANEL

    Hy-IQ Surface Cleaner Hy-IQ Surface Cleaner

  • INGREDIENTS AND APPEARANCE
    HY-IQ SURFACE CLEANER 
    hy-iq water spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76701-361
    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:76701-361-26473.176 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/21/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/21/2021
    Labeler - HAND SANITIZER LLC (117473019)
    Establishment
    NameAddressID/FEIBusiness Operations
    HAND SANITIZER LLC117473019manufacture(76701-361) , pack(76701-361) , label(76701-361)