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.

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HORSEMAN'S DREAM FUNG-A-WAY TOPICAL FUNGICIDE SOLUTION

Drug Facts

Active Ingredients: Benzalkonium chloride 0.15%

Purpose: Skin wound cleaner

Purpose: skin wound cleaner

Uses:

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

Warnings

For external veterinary use only.

Not 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.

Directions

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

Apply daily until hair begins to grow.

Rinse treated areas 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

CORONA

SINCE 1906

TOPICAL FUNGICIDE

FUNG-A-WAY

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

800-690-9908

www.mannapro.com

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HORSEMANS DREAM FUNG-A-WAY 
benzalkonium chloride solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86077-1040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.15 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:86077-1040-6453.6 mL in 1 BOTTLE
2NDC:86077-1040-2907.2 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/02/2017
Labeler - Manna Pro Products LLC (147666812)
Registrant - Manna Pro Products LLC (147666812)

Revised: 4/2024
Document Id: 8d1e0060-7bde-4f9f-a70c-24277329a9d8
Set id: 7edfd175-6c3d-471c-8d97-6143dfe939fb
Version: 19
Effective Time: 20240415
 
Manna Pro Products LLC