Label: BLU-KOTE VETERINARY ANTISEPTIC-PROTECTIVE WOUND DRESSING- sodium propionate, gentian violet, acriflavine liquid

  • NDC Code(s): 15878-211-11, 15878-211-21
  • Packager: H. W. Naylor Company Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 4, 2013

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  • Active Ingredients

    Sodium Propionate 9.1%, Gentian Violet 1%, Acriflavine 0.15%

  • Purpose

    Effective treatment for FUNGUS INFECTION, SURFACE WOUNDS, CUTS, GALLS, CHAFES, ABRASIONS, MOIST LESIONS, ITCHY FUNGUS, ECZEMA and SORES: HOOF, FOOT AND PAD SORES for HORSES and DOGS.

  • Directions

    PAINT ON HORSES and DOGS.

    Clean and dry affected area.

    Apply BLU-KOTE with attached applicator morning and night or as required.

  • Safety

    CAUTION: In case of serious burns, deep or puncture wounds, consult veterinarian.

    If redness, irritation or swelling persists or increases, discontinue use and consult veterinarian.

    Keep away from eyes, mouth, nostrils and mucous membranes.

    Do not apply to large areas of broken skin.

    BLUE-KOTE stains anything, wet or dry.

    PREVENT DOG FROM LICKING TREATED AREA.

    DO NOT APPLY TO CATS.

    NOT FOR USE ON HORSES INTENDED FOR FOOD.

    FOR ANIMAL USE ONLY.

  • KEEP FROM REACH OF CHILDREN

  • Other Ingredients

    Water, Urea, Glycerine, Isopropyl Alcohol 47% by volume.

  • Principal Display Panel

    Dr. Naylor®

    BLU-KOTE®

    Veterinary Antiseptic - Protective Wound Dressing
    Germicidal Fungicidal

    Four Fluid Ozs. (118 ml)

    H.W. NAYLOR CO., INC.
    www.drnaylor.com
    Morris, N.Y. 13808
    U.S.A.

    QUICK-DRYING DEEP-PENETRATING
    Effective against both bacterial and fungus infections most common in skin lesions of domestic animals.

    Label
  • INGREDIENTS AND APPEARANCE
    BLU-KOTE VETERINARY ANTISEPTIC-PROTECTIVE WOUND DRESSING  
    sodium propionate, gentian violet, acriflavine liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:15878-211
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Sodium Propionate (UNII: DK6Y9P42IN) (Propionic Acid - UNII:JHU490RVYR) Sodium Propionate90 mg  in 1000 mL
    Gentian Violet (UNII: J4Z741D6O5) (Gentian Violet Cation - UNII:3GVJ31T6YY) Gentian Violet10 mg  in 1000 mL
    Acriflavine (UNII: 1T3A50395T) (Acriflavine - UNII:1T3A50395T) Acriflavine1.7 mg  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Urea (UNII: 8W8T17847W)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15878-211-11118 mL in 1 BOTTLE, WITH APPLICATOR
    2NDC:15878-211-21118 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1964
    Labeler - H. W. Naylor Company Inc. (002080190)
    Establishment
    NameAddressID/FEIBusiness Operations
    H. W. Naylor Company Inc.002080190API MANUFACTURE, MANUFACTURE
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