FDA.reportPublic FDA data

Quality Choice Antifungal Tolnaftate Liquid Spray

Manufacturer
Chain Drug Marketing Association
Effective date
2026-06-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-06-11 05:11:14

Label at a glance#

ProductTolnaftate
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

proven clinically effective in the treatment of 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 layer over affected area twice daily (morning and 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 use daily for 4 weeks if condition persists, consult a doctor to prevent athlete's foot, a...

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 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.

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

  • irritation occurs
  • no improvement within 4 weeks

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)
  • 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
  • use daily for 4 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 the scalp or nails

Other information

OTHER SAFETY INFORMATION

store between 20° and 30°C (68° and 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

BHT, isobutane (propellant), PPG-12-buteth-16, SD alcohol 40-B (36% w/w)

Questions?

OTC - QUESTIONS SECTION

Call 1-248-449-9300

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Quality Choice

Athlete's

Foot Relief

Antifungal Liquid Spray

Tolnaftate 1%

Cures most athlete's foot & prevents recurrences

Relieves itching, cracking & burning

NET WT

5.3 OZ (150 g)

antifungal tolnaftate liquid sprayantifungal tolnaftate liquid spray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63868-798-532026-01-29C16284748780-149896155-a926-586f-e063-e6dba90add90Quality Choice Antifungal Tolnaftate Liquid Spray
63868-798-532026-01-29C16284748780-149896155-a926-586f-e063-e6dba90add90Quality Choice Antifungal Tolnaftate Liquid Spray

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-798-53GM - Gram63868-79823248be6-7c4f-4458-8d69-f10958a99d4d12022-11-07

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
63868-79863868-798-53

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
ISOBUTANEBXR49TP611IACT
PPG-12-BUTETH-1658CG7042J1IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-12-11full-release2026-06-01 00:42:30

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
TolnaftateANTIFUNGAL LIQUID SPRAYChain Drug Marketing Associationaa97d2ca-bcf4-3ee1-e053-2a95a90a748d2026-06-09WarningsExact identifier
ndc (package): 63868-798-53
ndc (product): 63868-798
ndc11 (package): 63868079853
spl id: 53d7b662-15a0-8548-e063-6294a90a9ff8
spl set id: aa97d2ca-bcf4-3ee1-e053-2a95a90a748d

Reported adverse events (FAERS/openFDA)#

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