CLEAR COUGH- potassium iodide and ammonium chloride solution 
Medivet Pty Ltd

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.

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Directions For Use

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

Potassium Iodide  20 g/L

Ammonium Chloride 20 g/L

Uses

Clear Cough is a dietary supplement for horses.

Warnings

 For Animal Use only.

Inactive Ingredients

Water  and  Glycerin.

Keep Out of reach of Children

Keep Out of reach of Children

Package Label Principal Display Panel

clear cough

Manufactured By :

Stable Care

Lot 2 3B East Road

Pearcedale VIC 3912 Australia

Manufactured For:

Medivet Veterinary Supplies

U4A 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
(Air conditioning).
Protect from light.
DO NOT refrigerate or freeze






CLEAR COUGH 
potassium iodide and ammonium chloride solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51083-102
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:51083-102-01 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

Revised: 11/2012
Document Id: 6d12fc97-565f-49c6-b4c7-1c059715f379
Set id: 228cf65c-50d2-4aed-9e8b-fc35633e43bd
Version: 5
Effective Time: 20121129
 
Medivet Pty Ltd