FDA.reportPublic FDA data

Target Antifungal Tolnaftate 1% Liquid Spray

Manufacturer
Target Corporation
Effective date
2026-09-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-25 02:01:49

Label at a glance#

ProductTolnaftate
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis) prevents the recurrence of most athlete's foot with daily use for effective relief of itching, cracking and burning

Dosage and administration

wash affected area and dry thoroughly shake can well and spray a thin a layer of the product over affected area twice daily (morning and night) or as directed by a doctor to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night) supervise children in the use of this product for athlete's foot: pay special attention to spaces between the t...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • prevents the recurrence of most athlete's foot with daily use
  • for effective relief of itching, cracking and burning

Warnings

WARNINGS SECTION

For external use only.

Extremely Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire, sparks, and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • avoid spraying in eyes
  • use only as directed
  • intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • there is no improvement within 4 weeks.

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 a layer of the product over affected area twice daily (morning and night) or as directed by a doctor
  • to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night)
  • supervise children in the use of this product
  • for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
  • for athlete's foot and ringworm, use daily for 4 weeks
  • if condition persists, consult a doctor
  • this product is not effective on the scalp or nails

Other information

OTHER SAFETY INFORMATION

  • store between 20º and 30ºC (68º and 86ºF)
  • if nozzle clogs, clean with a pin

Inactive ingredients

INACTIVE INGREDIENT SECTION

ISOBUTANE, SD ALCOHOL 40-B, PPG-12-BUTETH-16, BHT

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to active ingredient in

Tinactin Liquid Spray

Soothing

Antifungal

Liquid Spray

Tolnaftate 1% / Antifungal

  • Cures most athlete's foot and

prevents recurrences

  • Comforts and refreshes

Relieves Itching,

Cracking

& Burning

NET WT. 5.3 OZ. (150 g)

cartoncarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130034197017756GTIN-13: 0034197017756
EAN-13: 0034197017756
GTIN-12: 034197017756
UPC-A: 034197017756
GTIN storage (14 digits): 00034197017756		Target_upup_Antifungal Tolnaftate Liquid Spray.jpg

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-20382442-203-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOLNAFTATE06KB629TKVACTIB
ALCOHOL3K9958V90MIACT
BHT1P9D0Z171KIACT
PPG-12-BUTETH-1658CG7042J1IACT
ISOBUTANEBXR49TP611IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-06-22monthly-update2026-07-17 21:35:08
22025-11-06full-release2026-06-01 01:42:32
12025-05-27full-release2026-06-01 01:02:03

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
54dae738-94db-7ad8-e063-6294a90abdfe365f6f60-e056-51bd-e063-6294a90ad01e2026-06-22WarningsExact identifier
spl set id: 365f6f60-e056-51bd-e063-6294a90ad01e

Reported adverse events (FAERS/openFDA)#

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