CONZOL 1 %- micaonazole spray 
MWI

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Conzol 1%
(miconazole nitrate)
Lotion & Spray

Topical antifungal agent for dogs and cats.

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


Not for Use in Humans
Keep Out of Reach of Children


Approved by FDA under ANADA # 200-362

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.

ACTIVE INGREDIENT:
Miconazole Nitrate...........1.15%
(equivalent to 1% miconazole base by weight)

STORAGE:

Store at controlled room temperature between 15°-30°C (59°-86°F). Keep container tightly closed when not in use.

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.

CONTACT INFORMATION:

To report suspected adverse events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact First Priority, Inc. at (800) 650-4899 or www.prioritycare.com. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae

Distributed by: MWI
Boise, ID 83705
www.VetOne.net
Rev. 04/23

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Approved by FDA under ANADA # 200-362

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60 mL bottle/case label

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120 mL bottle/case label

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240 mL bottle/case label

image of 240 mL bottle label - Front panelimage of 240 mL bottle label - Inside panel

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CONZOL  1 %
micaonazole spray
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:13985-596
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE11.5 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:13985-596-6072 in 1 CASE
160 mL in 1 BOTTLE, DROPPER
2NDC:13985-596-1272 in 1 CASE
2120 mL in 1 BOTTLE, SPRAY
3NDC:13985-596-2472 in 1 CASE
3240 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANADAANADA20036209/21/2023
Labeler - MWI (019926120)
Registrant - FIRST PRIORITY INCORPORATED (179925722)
Establishment
NameAddressID/FEIBusiness Operations
FIRST PRIORITY INCORPORATED179925722manufacture

Revised: 9/2023
Document Id: f72b9e3a-d8b6-4514-b2cc-1a6290dcbff6
Set id: ef1c9931-ce9d-4cf6-ac3f-7180d787e4dc
Version: 4
Effective Time: 20230921
 
MWI