Uroeze

Dosage Form: FOR ANIMAL USE ONLY
Uroeze® 400

Each 0.65 g (1/4 level teaspoonful) contains: Ammonium Chloride 400 mg in a palatable protein base.

INDICATION

For use as a urinary acidifier in cats and dogs.

CAUTION: Federal law (USA) restricts this drug to use by on the order of a licensed veterinarian.

Warning

Do not administer to animals with severe liver or kidney damage or to animals exhibiting acidosis.

CAUTION: May cause gastric mucosal irritation.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

STORE AT CONTROLLED ROOM TEMPERATURE OF 15°- 30°C (59°- 86°F).

DOSAGE

The suggested dosage of Uroeze for adult cats and dogs is 0.32 - 0.65 g (1/8 - 1/4 level teaspoonful) per 10 lbs. (4.5 kg) body weight twice daily with food. Daily dose may vary with different diets depending on alkalinity of diet. Dosage should be adjusted to maintain urine pH consistently below 6.6. Not intended for use in kittens.

ID# 854004

301599-02

Mfg. by:

Virbac AH, Inc. • P.O. Box 162059

Fort Worth, TX 76161 • (800) 338-3659

PRINCIPAL DISPLAY PANEL - 4 oz Bottle Label

NDC 051311-850-04

Uroeze® 400

Each 0.65 g (1/4 level teaspoonful) contains:

Ammonium Chloride 400 mg

in a palatable protein base.

INDICATION: For use as a urinary

acidifier in cats and dogs.

4 oz

CAUTION: Federal law (USA) restricts this drug to use

by or on the order of a licensed veterinarian.

Virbac

ANIMAL HEALTH

Mfg. by:

Virbac AH, Inc. • P.O. Box 162059

Fort Worth, TX 76161 • (800) 338-3659

Uroeze  ammonium chloride  powder

Product Information Product Type PRESCRIPTION ANIMAL DRUG NDC Product Code (Source) 51311-850 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ammonium chloride (ammonia) ammonium chloride 400 mg  in 0.65 g

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color BROWN Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 51311-850-04 113.3981 g In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		01/26/2010

Labeler - Virbac AH, Inc. (131568396)

Establishment
Name	Address	ID/FEI	Operations
Virbac Bridgeton		808558100	MANUFACTURE

Revised: 01/2010Virbac AH, Inc.