Maximum Strength Antifungal Liquid

Manufacturer
Premier Brands of America Inc.
Effective date
2024-05-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:01:28

Label at a glance#

ProductMaximum Strength Antifungal Liquid
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

For the treament of athlete's foot (tinea pedis) and ring worm (tinea corporis). For effective relief of itching, scaling, cracking, burning, and redness.

Dosage and administration

wash 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 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% w/w

​Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • For the treament of athlete's foot (tinea pedis) and ring worm (tinea corporis).
  • For effective relief of itching, scaling, cracking, burning, and redness.

Warnings

WARNINGS SECTION

For external use only.

Flammable

OTC - DO NOT USE SECTION

  • Keep away from fire or flame.

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 or if there is no improvement in 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 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 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.
  • this product is not effective on the scalp or nails.

​Other information​

OTHER SAFETY INFORMATION

  • store at room temperature 15°-30°C (59° - 86°F).
  • keep tightly closed when not in use.

​Inactive ingredient

INACTIVE INGREDIENT SECTION

Acetone, Water, Propylene Glycol, Tocopherol Acetate.

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

premier solutions

MAXIMUM STRENGTH

ANTIFUNGAL

LIQUID

TOLNAFTATE 1%/ANTIFUNGAL

SHAKE WELL BEFORE USE

Maximum strength

Cures & prevents athlete's foot

Brush-on applicator

Treats fungus on skin & under the nails

1.0 FL OZ (30 mL)

BoxBoxLabelLabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56104-900MAXIMUM STRENGTH ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [PREMIER BRANDS OF AMERICA INC.]1Unmatched20240601_19ada9c8-2f21-8701-e063-6394a90a39c6.zip

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
56104-90056104-900-30

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

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
380f46bc-c522-6dfe-e063-6394a90acf7919ada9c8-2f21-8701-e063-6394a90a39c62025-06-21WarningsExact identifier
spl set id: 19ada9c8-2f21-8701-e063-6394a90a39c6

Reported adverse events (FAERS/openFDA)#

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