Mint Blast-Foot and Shoe Antifungal Spray

Manufacturer
SANSAR, LLC
Effective date
2025-11-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:23

Label at a glance#

ProductMint Blast Foot and Shoe Antifungal
Active ingredientUNDECYLENIC ACID
Label structure13 sections

Indications and uses

• For the treatment of most athlete's foot, jock Itch and ringworm. • Odor control & Deodorizer for shoes & feet.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic acid 10%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses 

INDICATIONS & USAGE SECTION

• For the treatment of most athlete's foot, jock Itch and ringworm.
• Odor control & Deodorizer for shoes & feet.

Warnings

WARNINGS SECTION

For External use only.

Do not apply to wounds or damaged skin.

OTC - PREGNANCY OR BREAST FEEDING SECTION

lf pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

When using this product: Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor: If irritation occurs or if there is no improvement within 4 weeks.

If swallowed, get medical help or contact a Poison control centre right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Read all warnings and directions. Use only as directed.

For use on feet:

• Clean the affected area with soap & water and dry thoroughly.
• Shake the bottle well before use.
• Spray a thin layer of the product over covered.
• For athlete's foot, keep toes dry, wear ventilated shoes,and change socks daily.

For use on shoes:

• If you have just worn your Shoes, Take Off your Shoes & Allow them to sit For 15+ Minutes.
• Shake the Bottle lightly and Spray 1-2 Times In each Shoe.
• Allow Shoes to Dry for 10+ Minutes Before Putting Back On.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerol, Tea Tree Oil, Eucalyptus Oil, Peppermint Oil, Spearmint Oil, Clove Bud Oil, Vltamin E.

Other Information

SPL UNCLASSIFIED SECTION

Store at 15-30°C(59°-86°F)
Keep cap on bottles when not in use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foot Shoe Spray Label (Tea Tree Mint Blast)_page-0001Foot Shoe Spray Label (Tea Tree Mint Blast)_page-0001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1251011undecylenic acid 10 % Topical SprayPSN1
1251011undecylenic acid 100 MG/ML Topical SpraySCD1
1251011undecylenic acid 10 % Topical SpraySY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83691-013-01Mint Blast Foot and Shoe Antifungal120 mL in 1 BOTTLE, SPRAYSPRAY1201

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83691-01383691-013-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mint Blast Foot and Shoe AntifungalUNDECYLENIC ACID 10%SANSAR, LLCf7fcac19-7b72-4b7a-a28e-669a0eebec9c2025-11-15WarningsExact identifier
ndc (package): 83691-013-01
ndc (product): 83691-013
ndc11 (package): 83691001301
spl id: 7916c194-6aa1-4941-90b7-ff6930442e83
spl set id: f7fcac19-7b72-4b7a-a28e-669a0eebec9c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.