FDA.reportPublic FDA data

Exchange Select Antifungal Tolnaftate Powder Spray

Manufacturer
ARMY & AIR FORCE EXCHANGE SERVICE
Effective date
2025-12-09
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
monthly-update
Hydrated at
2026-06-03 17:45:39

Label at a glance#

ProductTolnaftate
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris) can prevent recurrence of most athlete's foot relieves symptoms of athlete's foot, including itching, burning, cracking and chafing associated with jock itch

Dosage and administration

wash affected area and dry thoroughly shake can well and spray a thin layer over affected area twice daily (morning and night) or as directed by a doctor supervise children in the use of this product for athlete's foot, pay special attention to spaces between toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily use daily for 4 weeks for athlete's foot, ringworm and for jock itch...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris)
  • can prevent recurrence of most athlete's foot
  • relieves symptoms of athlete's foot, including itching, burning, cracking and chafing associated with jock itch

Warnings

WARNINGS SECTION

For external use only.

Flammable:

SAFE HANDLING WARNING SECTION

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120°F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

​When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes or mouth
  • use only as directed

​Stop use and ask a doctor if

OTC - STOP USE SECTION

  • no improvement within 4 weeks for athlete's foot, ringworm and 2 weeks for jock itch
  • irritation occurs

​Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over affected area twice daily (morning and

night) or as directed by a doctor

  • supervise children in the use of this product
  • for athlete's foot, pay special attention to spaces between toes; wear

well-fitting, ventilated shoes and change shoes and socks at least once daily

  • use daily for 4 weeks for athlete's foot, ringworm and for jock itch use daily

for 2 weeks

  • if condition persists, consult a doctor
  • to prevent athlete's foot, apply once or twice daily (morning and/or night)
  • this product is not effective on scalp or nails
  • in case of clogging, clear nozzle under running water

Other information

OTHER SAFETY INFORMATION

store between 20º and 30ºC (68ºF and 86º)

Inactive ingredient

INACTIVE INGREDIENT SECTION

BHT, isobutane (propellant), PPG-12-buteth-16, SD Alcohol 40-B (14% w/w), talc

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

exchange select

ATHLETE'S

FOOT

ANTIFUNGAL
tolnaftate 1%

  • CURES & PREVENTS
    MOST ATHLETE'S FOOT
  • RELIEVES ITCHING &
    BURNING

Powder Spray

NET WT 4.6 OZ (130 g)

Exchange Select_Antifungal Tolnaftate Powder Spray_50-060ES.jpgExchange Select_Antifungal Tolnaftate Powder Spray_50-060ES.jpg

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55301-13255301-132-46

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ISOBUTANEBXR49TP611IACT
PPG-12-BUTETH-1658CG7042J1IACT
ALCOHOL3K9958V90MIACT
TALC7SEV7J4R1UIACT
TOLNAFTATE06KB629TKVACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-10-30monthly-update2026-06-03 17:39:07
62024-12-06full-release2026-06-01 00:40:47

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
4c5ccfb4-05ae-7e59-e063-6294a90a5d612693b442-b7ce-482e-bd47-bba370dfb98e2026-03-06WarningsExact identifier
spl set id: 2693b442-b7ce-482e-bd47-bba370dfb98e

Reported adverse events (FAERS/openFDA)#

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