Topical Fungicide: Product Information

TOPICAL FUNGICIDE- benzalkonium chloride solution
First Priority, Incorporated

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.

For Control of Summer Itch, Girth Itch, Ringworm

For Cattle, Sheep, Goats, Horses, Dogs and Cats

For Animal Use Only • 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, girth itch, 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.

CAUTION:

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

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ACTIVE INGREDIENT:

Benzalkonium chloride ………………….0.15%

Other Ingredients:

Allantoin

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) Reorder No. TP080PC

32 fl oz (960 mL) Reorder No. TP081PC

Priority Care is a registered trademark of First Priority, Inc.

Made in U.S.A.

Manufactured By: FIRST PRIORITY, INC., Elgin, IL 60123

www.prioritycare.com

NOT RETURNABLE IF OUTDATED

16 fl oz (473 mL)

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32 fl oz (960 mL)

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TOPICAL FUNGICIDE
benzalkonium chloride solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:58829-195
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 3.09 mg in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58829-195-16 12 BOTTLE, SPRAY in 1 CASE contains a BOTTLE, SPRAY
1 473 mL in 1 BOTTLE, SPRAY This package is contained within the CASE (58829-195-16)
2 NDC:58829-195-32 12 BOTTLE, SPRAY in 1 CASE contains a BOTTLE, SPRAY
2 960 mL in 1 BOTTLE, SPRAY This package is contained within the CASE (58829-195-32)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/01/2013
Labeler — First Priority, Incorporated (179925722)
Establishment
Name Address ID/FEI Operations
First Priority, Incorporated 179925722 manufacture, label

Revised: 11/2016 First Priority, Incorporated

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