Label: CUPRIC SULFATE PENTAHYDRATE- cupric sulfate powder, for solution

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 25, 2010

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  • ACTIVE INGREDIENT

    Active Ingredient: Cupric Sulfate [Powder for use in solution]

  • PURPOSE

    Purpose: Cupric Sulphate Pentahydrate powder is used as an aid in hoof rot management under veterinary guidance.

  • DO NOT USE

    Warnings:
    • Copper can be toxic to sheep. Do not allow animals to eat or drink the cupric sulphate powder or hoof bath solution.
    • Know the volume of the hoof bath and calculate the amount of cupric sulphate carefully.
    • Do not overdose by using more cupric sulphate than what is recommended by your veterinarian.
  • WHEN USING

    When Using this Product: By placing a clean water bath ahead of the treatment bath, animals will clean their hooves to some extent and keep the treatment bath clean longer. Hoof baths should only be part of an overall program that includes proper nutrition, regular hoof trimming, and hoof injury prevention.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • QUESTIONS

    Questions?: 1-800-567-7455 (24/7-Emergency Spill Line) or 1-905-878-8432

  • Cupric Sulfate Labels

    Drug Facts Label
    Front Package Label
    Front Package Label Text
  • INGREDIENTS AND APPEARANCE
    CUPRIC SULFATE PENTAHYDRATE 
    cupric sulfate powder, for solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51044-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Cupric Sulfate (UNII: LRX7AJ16DT) (Cupric Cation - UNII:8CBV67279L) Cupric Cation0.4 kg  in 1.6 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51044-101-2525 kg in 1 BAG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2008
    Labeler - Fondel Chemicals Ltd. (201786790)
    Registrant - Fondel Chemicals Ltd. (201786790)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fondel Chemicals Ltd.201786790manufacture, label
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