HORSEMANS DREAM FUNG-A-WAY- benzalkonium chloride solution
Manna Pro Products LLC

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: Benzalkonium chloride 0.15%

Purpose: Skin wound cleaner

Purpose: skin wound cleaner


For use on horses and dogs as an aid in the control of ringworm, summer itch, girth itch, and other fungal infections.


For external veterinary use only.

Nor for human use.

Not for use on animals intended for food

When using this product avoid eyes and 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, seek medical attention.


Soak affected area liberally with topical fungicide solution. Leave treated area uncovered.

Apply daily until hair begins to grow.

Rinse treated ares with clear water before reapplying.

Results should be apparent in a matter of days. Care should be taken to minimize the animal’s ingestion of topical fungicide solution through self-grooming.

Note: Efficiency is neutralized by soap or detergent residues.

Inactive Ingredients:

Allantoin, Benzathonium Chloride, Carbamide, FD&C Yellow #5, FD&C Red #40, Purified Water


SINCE 1906



Aids in The Control Of Fungal Infections

– Topical Antiseptic to Help Control Ringworm, Summer Itch, Girt Itch, and Other Fungal Conditions.

– Protects and Soothes Irritated Skin

– Non-Staining

– For Use on Horses & Dogs

Manufactured For:

Manna Pro Products, LLC

707 Spirit 40 Park Drive

Suite 150

St. Louis, MO 63005


16oz label 2021
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16oz label 2021
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32oz label 2021
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32oz label 2021
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benzalkonium chloride solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86077-1040
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
# Item Code Package Description Multilevel Packaging
1 NDC:86077-1040-6 453.6 mL in 1 BOTTLE None
2 NDC:86077-1040-2 907.2 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/02/2017
Labeler — Manna Pro Products LLC (147666812)
Registrant — Manna Pro Products LLC (147666812)

Revised: 05/2022 Manna Pro Products LLC 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 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.

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