Label: HY-IQ OPEN WOUND CARE- 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 29, 2021

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  • ACTIVE INGREDIENT

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

    Hydrogen Cation .77%

  • PURPOSE

    ANTISEPTIC

  • USES

    FOR THE CLEANING OF MINOR ACUTE WOUNDS SUCH AS CUTS, GRAZES, SKIN ABRASIONS AND SORES.

  • 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

  • DIRECTIONS

    SPRAY ENOUGH Hy-IQ® OPEN WOUND CARE TO DAMPEN THE WOUND. ALLOW TO DRY, THEN DRESS WOUND WITH APPROPRIATE, STERILE DRESSING.

  • OTHER SAFETY INFORMATION

    STORE UNDER 110 F (43 C)

  • INACTIVE INGREDIENT SECTION

    WATER UREA

  • HY-IQ OPEN WOUND CARE

    HY-IQ OPEN WOUND CARE

  • INGREDIENTS AND APPEARANCE
    HY-IQ OPEN WOUND CARE 
    hy-iq water spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76701-363
    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:76701-363-0150.275 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/29/2021
    2NDC:76701-363-08237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/29/2021
    Labeler - HAND SANITIZER LLC (117473019)
    Establishment
    NameAddressID/FEIBusiness Operations
    HAND SANITIZER LLC117473019manufacture(76701-363) , label(76701-363) , pack(76701-363)