Target Maximum Strength Antifungal Liquid

Manufacturer
Target Corporation
Effective date
2026-09-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-29 01:03:49

Label at a glance#

ProductAntifungal Liquid
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, burning, cracking, redness and scaling

Dosage and administration

clean the affected area and dry thoroughly apply a thin layer of the product over the 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 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...

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, burning, cracking, redness and scaling

Warnings

WARNINGS SECTION

For external use only.

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 contact with the eyes.

Stop use and consult 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 accidental ingestion occurs, get medical help or contact a Poison Control Center right away.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area and dry thoroughly
  • apply a thin layer of the product over the 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 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 longer, consult a doctor
  • to prevent athlete's foot: wash the feet and dry thoroughly; apply a thin layer of the product to the feet once or twice daily (morning and/or night)
  • this product is not effective on the scalp or nails

​Other information​

OTHER SAFETY INFORMATION

  • SHAKE WELL BEFORE USE
  • store at room temperature 15°-30°C (59° - 86°F)
  • protect from freezing; if freezing occurs, warm to room temperature
  • keep tightly closed when not in use

​Inactive ingredient

INACTIVE INGREDIENT SECTION

Acetone, Propylene Glycol,Tocopherol Acetate, Water

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

Fungi-Nail Anti-Fungal Liquid

Maximum Strength

Antifungal

Liquid

Tolnaftate 1%/ Antifungal

  • Proven clinically effective in

the treatement of fungus on

fingers, toes, and skin around nails

  • Prevents the recurrence of most athlete's foot with

daily use

  • Relieves itching, burning, and scaling

**This product is not effective

on the scalp or nails

1 FL.OZ. (30 mL)

cartoncarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130034197018913GTIN-13: 0034197018913
EAN-13: 0034197018913
GTIN-12: 034197018913
UPC-A: 034197018913
GTIN storage (14 digits): 00034197018913
Target_upup_Antifungal Liquid Solution_53-218TG.jpg

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-99882442-998-01

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-08-15full-release2026-06-01 01:10:36

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
3c6dd780-6ac8-d88d-e063-6394a90a11243c6dd772-0d26-b659-e063-6294a90a5bf82025-08-15WarningsExact identifier
spl set id: 3c6dd772-0d26-b659-e063-6294a90a5bf8

Reported adverse events (FAERS/openFDA)#

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