HORSEMANS DREAM FUNG-A-WAY: Product Information

HORSEMANS DREAM FUNG-A-WAY — benzalkonium chloride solution
SUMMIT INDUSTRIES

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.

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

FUNGAWAY_LABEL_PDP
(click image for full-size original)

FUNGAWAY_LABEL_FACTS
(click image for full-size original)

HORSEMANS DREAM FUNG-A-WAY
benzalkonium chloride solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC: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
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC: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: 09/2010 SUMMIT INDUSTRIES

VetLabel.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by VetLabel.com. Every individual animal healthcare product label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

Our database mirrors the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. VetLabel.com provides the full animal health subset of the FDA's repository. Veterinary information provided here is not intended as a substitute for direct consultation with a qualified veterinary professional.

Terms of Use | Copyright © 2022. All Rights Reserved.