Label: EXOCOUGH- potassium iodide and ammonium chloride solution

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

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 August 25, 2016

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  • Active

    POTASSIUM IODIDE 20 g / L
    AMMONIUM CHLORIDE  20 g /L 

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  • Inactive ingrdients

    Glycerin, H20 Distilled Water, Benzoyl Alcohol and Red Dye 

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  • Purpose of use

    Equine Health Supplement  

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  • Do not use

    Not to be used for horses in human consumption.

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  • Product label
  • INGREDIENTS AND APPEARANCE
    EXOCOUGH 
    potassium iodide and ammonium chloride solution
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86070-001
    Route of Administration ORAL
    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 CATION 20 g  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Product Characteristics
    Color red Score     
    Shape Size
    Flavor APPLE Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:86070-001-20 20 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 07/07/2016
    Labeler - Nu-Vet Pty Ltd (750770047)
    Establishment
    Name Address ID/FEI Business Operations
    Stable Care Pty 753177401 manufacture
    Establishment
    Name Address ID/FEI Business Operations
    G AMPHRAY LABORATORIES 862288982 api manufacture
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