CONZOL 1 %- micaonazole spray

Conzol by

Drug Labeling and Warnings

Conzol by is a Animal medication manufactured, distributed, or labeled by MWI, FIRST PRIORITY INCORPORATED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INFORMATION FOR OWNERS/CAREGIVERS

Topical antifungal agent for dogs and cats.

DESCRIPTION:

Conzol™ Lotion, 1% (miconazole nitrate) & Conzol™ Spray, 1% (miconazole nitrate) is a synthetic antifungal agent for use in dogs and cats.  It contains: 1.15% miconzole nitrate (equivalent to 1% miconzole base by weight), polyethylene glycol 400, ethyl alcohol 55%.

INDICATIONS:

Conzol™ Lotion, 1% (miconzole nitrate) & Conzol™ Spray, 1% (miconzole nitrate) is indicated for the treatment of fungal infections in dogs and cats caused by Microsporum canis, Microsporum gypseum​, and Trichophyton mentagrophytes.

PRECAUTIONS:

In the event of sensitization or irritation due to Conzol™ Lotion, 1% (miconazole nitrate) & Conzol™ Spray, 1% (miconazole nitrate), treatment should be discontinued. Avoid contact with eyes, since irritation may result. Wash hands thoroughly after administration to avoid spread of fungal infection.

DOSAGE AND ADMINISTRATION:

Accurate diagnosis of the infecting organism is essential. Identification should be made either by direct microscopic examination of a mounting of infected tissue in a solution of potassium hydroxide, or by culture on an appropriate medium.

Lotion: Apply a light covering of Conzol™ Lotion, 1% (miconazole nitrate) to affected areas, once daily, for 2 to 4 weeks.  Application is best accomplished using a gauze pad or cotton swab.

Spray: Spray affected areas from a distance of 2 to 4 inches to apply a light covering, once daily for 2 to 4 weeks.  Do not allow pet to contact finished wood surfaces until pet is thoroughly dried.

Medication must be continued until the infecting organism is completely eradicated as indicated by appropriate clinical or laboratory examination. If no improvement is noticed within 2 weeks, diagnosis should be re-evaluated. Difficult cases may require treatment for 6 weeks.

General measures in regard to hygiene should be observed to control sources of infection or reinfection. Clipping of hair around and over the sites of infection should be done at the start of treatment and again as necessary.

HOW SUPPLIED:

Lotion:

Conzol™ Lotion, 1% (miconazole nitrate) is available in 30 and 60 mL bottles with droppers.

Spray:

Conzol™ Spray, 1% (miconazole nitrate) is available in 120 mL & 240 mL bottles with spray misters.

CAUTION:

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Rev. 03/14 (60 mL)

Rev. 02/14 (120 mL & 240 mL)

Distributed by: MWI

Boise, ID 83705

(888)694-8381

www.VetOne.net

ANADA# 200-362,

Approved by FDA

60 mL bottle/case label

120 mL bottle/case label

240 mL bottle/case label

INGREDIENTS AND APPEARANCE

CONZOL  1 %
micaonazole spray

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 13985-596
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	11.5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13985-596-60	72 in 1 CASE
1		60 mL in 1 BOTTLE, DROPPER
2	NDC: 13985-596-12	72 in 1 CASE
2		120 mL in 1 BOTTLE, SPRAY
3	NDC: 13985-596-24	72 in 1 CASE
3		240 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANADA	ANADA200362	08/28/2014

Labeler - MWI (019926120)

Registrant - FIRST PRIORITY INCORPORATED (179925722)

Establishment
Name	Address	ID/FEI	Business Operations
FIRST PRIORITY INCORPORATED		179925722	manufacture