Horsemans Dream Fung-A-Way

Generic Name: benzalkonium chloride solution

Dosage Form: FOR ANIMAL USE ONLY
HORSEMAN'S DREAM FUNG-A-WAY TOPICAL FUNGICIDE SOLUTION 16 oz

Drug Facts

Active Ingredients                                 Purpose

Benzalkonium chloride 0.15%               Skin wound cleaner

purpose: skin wound cleaner

Uses:

For use on horses, dogs, and cats, as an aid in the control of summer itch, girth itch and ringworm

Warnings

For external veterinary use only

Nor for human use

Not for use on animals intended for food

When using this product

do not get into eyes or mucous membranes. If contact occurs, flush immediately with water.

Stop use and consult your veterinarian if

no improvement is noted within seven days.

Keep out of reach of children. In case of contact with eyes or mucous membranes, obtain medical attention for eye inflammation.

Directions

soak affected area liberally with topical fungicide solution.

Apply daily until hair begins to grow.

Leave treated area uncovered

Rinse treated ares with clear water before reapplying

Results should be apparent in a matter of days

Note: efficiency is neutralized by soap or detergent residues.

Inactive Ingredients:

Deionized water, carbamide, allantoin, quaternium-15, FC and C yellow no. 5, FD and C red no. 40

HORSEMAN'S DREAM

FUNG-A-WAY

Topical Fungicide Solution

-Aids in control of

-Summer itch

-girth itch-

-ringworm

for use on Horses, dogs, and cats

Manufactured Exclusively For:

Horseman's Dream Inc.

Forth Worth, TX 76126

Horsemans Dream Fung-A-Way  benzalkonium chloride  solution

Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 12090-1041 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.15 mL  in 100 mL

Inactive Ingredients Ingredient Name Strength WATER   UREA   ALLANTOIN   QUATERNIUM-15

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 12090-1041-6 453.6 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/17/2010

Labeler - SUMMIT INDUSTRIES (003279189)

Registrant - SUMMIT INDUSTRIES (003279189)

Establishment
Name	Address	ID/FEI	Operations
GDMI, INC		040646846	manufacture

Revised: 09/2010SUMMIT INDUSTRIES