Label: KOPERTOX- copper naphthenate liquid 

  • Label RSS
  • NDC Code(s): 0856-0752-01, 0856-0752-02
  • Packager: Fort Dodge Animal Health Div of Wyeth
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Animal Drug Application

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 09/14

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    WATER-RESISTANT PROTECTION WITHOUT BANDAGING

    RECOMMENDED as an aid in treating horses and ponies with thrush due to organisms susceptible to copper naphthenate.

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  • Ingredients:

    Copper Naphthenate..................................... 37.5% w/w

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  • INACTIVE INGREDIENT

    Inert Ingredients............................................ 62.5% w/w

    Total............................................................... 100%

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  • INFORMATION FOR OWNERS/CAREGIVERS

    FOR EXTERNAL USE ONLY

    For Animal Use Only.

    Keep Out of Reach of Children.

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  • GENERAL PRECAUTIONS

    CAUTION: Do not use in horses intended for human consumption.

    CAUTION: COMBUSTIBLE MIXTURE

    Use in a well-ventilated place.  Avoid fire, flame, sparks or heaters.

    If swallowed, do not induce vomiting, call physician immediately.  Avoid breathing vapor.  Avoid contact with skin and eyes.

    Keep out of reach of children and pets.

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  • GENERAL DIRECTIONS:

    Clean the hoof thoroughly, removing debris and necrotic material prior to application of KOPERTOX®. Apply daily to affected hoofs with a narrow paint brush (about 1") until fully healed. Caution: Do not allow runoff of excess KOPERTOX® onto hair since contact with KOPERTOX® may cause some hair loss.  Do not contaminate feed.

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  • STORAGE AND HANDLING

    Store at controlled room temperature 15° to 30°C (59° to 86°F).  Keep container tightly closed when not in use.

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  • INFORMATION FOR OWNERS/CAREGIVERS

    NOTE: KOPERTOX® is easily removed from hands, clothing and surfaces with light grade fuel oil or any type of lighter fluid.

    CONTAINS FOIL SEAL – REMOVE BEFORE USE.

    SHAKE WELL BEFORE USE.

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  • ADVERSE REACTIONS

    To report suspected adverse reactions or to obtain technical assistance, call 1-800-650-4899.

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  • Net Contents:

      8 oz (236 mL) Rev. 03-06 0754H  00826

    16 oz (473 mL) Rev. 02-14  0755J  30175500

    ANADA 200-304, Approved by FDA

    zoetis

    Distributed by:

    Zoetis Inc.

    Kalamazoo, MI 49007

    Manufactured by:

    First Priority, Inc.

    Elgin, IL 60123

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  • PRINCIPAL DISPLAY PANEL

    image of 236 mL bottle/case label

    Image of 236 mL bottle/case label

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  • PRINCIPAL DISPLAY PANEL

    Image of 473 mL bottle/case label (rev. 02-14)

    image of 473 mL bottle/case label

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  • INGREDIENTS AND APPEARANCE
    KOPERTOX 
    copper naphthenate liquid
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:0856-0752
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COPPER NAPHTHENATE (COPPER) COPPER NAPHTHENATE 0.825 g  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0856-0752-01 12 in 1 CASE
    1 236 mL in 1 BOTTLE, DISPENSING
    2 NDC:0856-0752-02 12 in 1 CASE
    2 473 mL in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANADA ANADA200304 03/01/2006
    Labeler - Fort Dodge Animal Health Div of Wyeth (149957656)
    Establishment
    Name Address ID/FEI Business Operations
    FIRST PRIORITY INCORPORATED 179925722 manufacture
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