Label: MUTIAN VETRESPONSA- care solution liquid

  • NDC Code(s): 73452-215-01, 73452-215-23
  • Packager: Nantong MUTIAN Biotechnology Co., Ltd
  • Category: OTC ANIMAL DRUG LABEL

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 January 10, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • WARNINGS AND PRECAUTIONS

    For external use only.
    For Dogs & Cats Use Only.
    Keep out of Reach of Children.
    Not for Injections.
    Discontinue use if irritation develops and contact your veterinarian.
    Always consult with a veterinarian for systemic conditions.

  • INDICATIONS & USAGE

    VETRESPONSATM is a one-stop, no rinse solution for immediate care of lacerations, cuts, abrasions, burns, and irritations. Use to debride and clean all dermal wounds.
    Apply amount of VETRESPONSATM directly on the wound to flush away dirt and debris.
    Thoroughly clean the wound. If dressing is bused, saturate it with VETRESPONSATM and apply a fresh moistened dressing one or more times daily as needed. Soak adherent dressings with VETRESPONSATM to ease removal. Repeat process until area is completely improved.

  • DOSAGE & ADMINISTRATION

    Proper amount per time.
    One or more times daily as needed.

  • ACTIVE INGREDIENT

    Sodium Chloride
    Hypochlorous Acid
    Sodium Hypochlorite

  • INACTIVE INGREDIENT

    Electrolyzed Oxygenated Water

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • STORAGE AND HANDLING

    Store at the room temperature away from direct sunlight and heat. Do not freeze.
    See bottle for date of expiation. No special disposal requirements.

  • PRINCIPAL DISPLAY PANEL

    Package Label

    Package Label

    Container Label

    Container Label

  • INGREDIENTS AND APPEARANCE
    MUTIAN VETRESPONSA 
    care solution liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:73452-215
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) Sodium Chloride0.0041 g  in 5 mL
    Hypochlorous Acid (UNII: 712K4CDC10) (Hypochlorous Acid - UNII:712K4CDC10) Hypochlorous Acid0.00075 g  in 5 mL
    Sodium Hypochlorite (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) Sodium Hypochlorite0.00015 g  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R) 4.995 mL  in 5 mL
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73452-215-2336 in 1 PACKAGE
    1NDC:73452-215-015 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/10/2020
    Labeler - Nantong MUTIAN Biotechnology Co., Ltd (554512204)
    Registrant - Nantong MUTIAN Biotechnology Co., Ltd (554512204)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nantong MUTIAN Biotechnology Co., Ltd554512204label, manufacture, api manufacture