TOPICAL FUNGICIDE- benzalkonium chloride solution

Topical Fungicide by

Drug Labeling and Warnings

Topical Fungicide by is a Animal medication manufactured, distributed, or labeled by Durvet, Inc., First Priority, Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Controls Fungal Problems

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

KEEP OUT OF REACH OF CHILDREN

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.

PRECAUTIONS

FOR ANIMAL USE ONLY

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)

INFORMATION FOR OWNERS/CAREGIVERS

Made in the U.S.A.

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

16 fl oz (473 mL)

32 fl oz (960 mL)

INGREDIENTS AND APPEARANCE

TOPICAL FUNGICIDE 
benzalkonium chloride solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-622
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	3.09 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30798-622-31	12 in 1 CASE
1		473 mL in 1 BOTTLE, SPRAY
2	NDC: 30798-622-34	12 in 1 CASE
2		960 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/12/2013

Labeler - Durvet, Inc. (056387798)

Establishment
Name	Address	ID/FEI	Business Operations
First Priority, Incorporated		179925722	manufacture, label, api manufacture