CLEAR COUGH- potassium iodide and ammonium chloride solution

Clear Cough by

Drug Labeling and Warnings

Clear Cough by is a Animal medication manufactured, distributed, or labeled by Medivet Pty Ltd, Stable Care Pty Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

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

INGREDIENTS AND APPEARANCE

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

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