Label: CLEAR COUGH- potassium iodide and ammonium chloride solution
- NDC Code(s): 51083-102-01, 51083-102-02, 51083-102-03
- Packager: Medivet Pty Ltd
- Category: OTC ANIMAL DRUG LABEL
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.
Updated November 29, 2012
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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 COUGH 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.
- Active Ingredients
- Inactive Ingredients
- Keep Out of reach of Children
Package Label Principal Display Panel
Manufactured By :
Lot 2 3B East Road
Pearcedale VIC 3912 Australia
Medivet Veterinary SuppliesU4A 101 Rookwood Rd,
Yagoona, NSW 2199, Australia
Meat Withholding Period (Horses): Zero
FIRST AID: If poisoning occurs,contact a doctor or Poisons Information Centre in your local area.
Disposal: Triple or (preferably) pressure rinse into medicated drench. Do not dispose of undiluted
chemicals on site. Break, crush or puncture and bury empty containers in a local authority landfill. If no landfill is available, bury the containers below 500mm in a disposal pit specifically marked and set up for this purpose clear of waterways, vegetation and roots.Empty containers and product should not be burnt.
Store below 25°C
Protect from light.
DO NOT refrigerate or freeze
INGREDIENTS AND APPEARANCE
potassium iodide and ammonium chloride solution
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51083-102 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 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:51083-102-01 1 L in 1 BOTTLE, PLASTIC 2 NDC:51083-102-02 2.5 L in 1 BOTTLE, PLASTIC 3 NDC:51083-102-03 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