TOPICAL FUNGICIDE- benzalkonium chloride solution 
Durvet, Inc.

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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Topical Fungicide

Controls Fungal Problems

For Control of Summer Itch, Foot Rot
Rain Rot, Girth Itch & Ringworm

KEEP OUT OF REACH OF CHILDREN

INDICATIONS:

For use on cattle, sheep, goats, horses, dogs and cats as an aid in the control of summer itch, foot rot, rain rot, ringworm and other fungal problems.

DIRECTIONS FOR USE:

Soak affected area liberally with TOPICAL FUNGICIDE solution. Apply daily until hair begins to grow. Leave treated areas uncovered.
Rinse treated areas with clear water before reapplying. Results should be apparent in a matter of days. If no improvement is noted within seven days, consult your veterinarian.

FOR ANIMAL USE ONLY

image of eye clock

ACTIVE INGREDIENT:

Benzalkonium Chloride ..........0.15% (w/w)

INACTIVE INGREDIENTS:

Purified Water, Allantoin, Artificial Color

CAUTION:

In case of contact with eyes or mucous membranes, flush immediately with water. Obtain medical attention for eye inflammation.

WARNING:

For external veterinary use only. Not for human use.

NOTE:

Efficiency is neutralized by soap or detergent residues.

STORAGE:

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

Net Contents:

16 fl oz (473 mL)

32 fl oz (960 mL)

Made in the U.S.A.

Manufactured for:
Durvet, Inc.
100 SE Magellan Drive
Blue Springs, MO 64014

16 fl oz (473 mL)

image of LBDUTP080_ISSU18XB07

32 fl oz (960 mL)

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TOPICAL FUNGICIDE 
benzalkonium chloride solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-622
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE3.09 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30798-622-3112 in 1 CASE
1473 mL in 1 BOTTLE, SPRAY
2NDC:30798-622-3412 in 1 CASE
2960 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/12/2013
Labeler - Durvet, Inc. (056387798)
Establishment
NameAddressID/FEIBusiness Operations
First Priority, Incorporated179925722manufacture, label, api manufacture

Revised: 2/2019
Document Id: 0e3227e3-ff55-4621-ab99-6ce4616b9521
Set id: 0de85075-f681-45f1-9f8f-aef19f9c2245
Version: 3
Effective Time: 20190221
 
Durvet, Inc.