Label: CLEAR SCOPE - potassium iodide and ammonium chloride solution

  • NDC Code(s): 51083-106-01, 51083-106-02, 51083-106-03
  • Packager: Medivet Pty Ltd
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 11/12

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

  • DOSAGE & ADMINISTRATION

    This product should not be used on pregnant or hyperthyroid animals.


    SHAKE WELL BEFORE USE
    Horses: 50mL /day for 20 days or as directed by your veterinary surgeon.

    CLEAR SCOPE may be administered by oral syringe or added to molasses and mixed well into nightly feed.For Severe or Chronic case: Ask your
    veterinarian to scope horses for confirmation of clearance of symptoms.Horses should be kept warm during treatment (double rugged) and left idle.

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  • Active Ingredients

    Potassium Iodide 20 g/L

    Ammonium Chloride  20 g/L

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  • Uses

    Clear Cough is a dietary supplement for horses.

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  • Warnings

    For Animal Use only.

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  • Inactive Ingredients

    Water  and  Glycerin.

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  • Keep Out of reach of Children

    Keep Out of reach of Children.

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  • INGREDIENTS AND APPEARANCE
    CLEAR SCOPE 
    potassium iodide and ammonium chloride solution
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51083-106
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) POTASSIUM IODIDE 20 g  in 1 L
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CHLORIDE 20 g  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51083-106-01 1 L in 1 BOTTLE, PLASTIC
    2 NDC:51083-106-02 2.5 L in 1 BOTTLE, PLASTIC
    3 NDC:51083-106-03 20 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 09/15/2012
    Labeler - Medivet Pty Ltd (757292763)
    Establishment
    Name Address ID/FEI Business Operations
    Stable Care Pty Ltd 753177401 analysis, manufacture, pack, api manufacture
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