OTC - ACTIVE INGREDIENT SECTION
Drug Facts
Active Ingredients Purpose
Benzalkonium chloride 0.15% Skin wound cleaner
HORSEMAN'S DREAM FUNG-A-WAY TOPICAL FUNGICIDE SOLUTION 16 oz
- Manufacturer
- SUMMIT INDUSTRIES | GDMI, INC
- Effective date
- 2010-09-17
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:39:21
Label at a glance#
ProductHORSEMANS DREAM FUNG-A-WAY
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
purpose: skin wound cleaner
INDICATIONS & USAGE SECTION
Uses:
For use on horses, dogs, and cats, as an aid in the control of summer itch, girth itch and ringworm
WARNINGS SECTION
Warnings
For external veterinary use only
Nor for human use
Not for use on animals intended for food
OTC - WHEN USING SECTION
When using this product
do not get into eyes or mucous membranes. If contact occurs, flush immediately with water.
OTC - STOP USE SECTION
Stop use and consult your veterinarian if
no improvement is noted within seven days.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of contact with eyes or mucous membranes, obtain medical attention for eye inflammation.
DOSAGE & ADMINISTRATION SECTION
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 INGREDIENT SECTION
Inactive Ingredients:
Deionized water, carbamide, allantoin, quaternium-15, FC and C yellow no. 5, FD and C red no. 40
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1012713 | benzalkonium chloride 1.5 MG/mL Topical Solution | PSN | 1 |
| 1012715 | Horseman's Dream FUNG-A-WAY 0.15 % Topical Solution | PSN | 1 |
| 1012715 | benzalkonium chloride 1.5 MG/ML Topical Solution [Horseman's Dream Fung-A-Way] | SBD | 1 |
| 1012713 | benzalkonium chloride 1.5 MG/ML Topical Solution | SCD | 1 |
| 1012715 | Horseman's Dream Fung-A-Way 0.15 % Topical Solution | SY | 1 |
| 1012715 | Horseman's Dream Fung-A-Way 1.5 MG/ML Topical Solution | SY | 1 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 12090-1041-6 | HORSEMANS DREAM FUNG-A-WAY | 453.6 mL in 1 BOTTLE | SOLUTION | 453.6 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 12090-1041 | HORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES] | 1 | 1 package rows | 20100920_06bdf766-5a3b-4248-8a2b-e03b2c2bf5d4.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BENZALKONIUM CHLORIDE | ACTIVE INGREDIENT | F5UM2KM3W7 | 1 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | 1 | |
| ALLANTOIN | INACTIVE INGREDIENT | 344S277G0Z | 1 | |
| QUATERNIUM-15 | INACTIVE INGREDIENT | E40U03LEM0 | 1 | |
| UREA | INACTIVE INGREDIENT | 8W8T17847W | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- HORSEMANS DREAM FUNG-A-WAY
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
- UREA
- ALLANTOIN
- QUATERNIUM-15
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 12090-1041 | 12090-1041-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| UREA | 8W8T17847W | IACT |
| ALLANTOIN | 344S277G0Z | IACT |
| QUATERNIUM-15 | E40U03LEM0 | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| QUATERNIUM-15 | QUATERNIUM-15 | E40U03LEM0 | LOTION / TOPICAL | NA | ||
| QUATERNIUM-15 | QUATERNIUM-15 | E40U03LEM0 | CREAM / TOPICAL | 0.02 %w/w | ||
| UREA | UREA | 8W8T17847W | TABLET, EXTENDED RELEASE / ORAL | 0.01 mg | ||
| UREA | UREA | 8W8T17847W | TABLET, EFFERVESCENT / ORAL | 60 mg | ||
| UREA | UREA | 8W8T17847W | SYSTEM / TOPICAL | 840 mg | ||
| UREA | UREA | 8W8T17847W | CREAM / VAGINAL | 0.64 %w/w | ||
| QUATERNIUM-15 | QUATERNIUM-15 | E40U03LEM0 | CREAM, AUGMENTED / TOPICAL | 0.1 %w/w | ||
| UREA | UREA | 8W8T17847W | INSERT / VAGINAL | 50 mg | ||
| UREA | UREA | 8W8T17847W | TABLET, COATED / ORAL | 0.02 mg | ||
| UREA | UREA | 8W8T17847W | DOUCHE / VAGINAL | 8 %w/w | ||
| ALLANTOIN | ALLANTOIN | 344S277G0Z | GEL / TOPICAL | 8 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.