Walgreens Athletes Foot Liquid Spray

Manufacturer
Walgreens
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:42:33

Label at a glance#

ProductWalgreens Athletes Foot
Active ingredientTOLNAFTATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

proven clinically effective in the treatment of most athlete’s foot (tinea pedis) and ringworm (tinea corporis)

helps prevent most athlete's foot with daily use

for effective relief of itching, burning and cracking

WARNINGS SECTION

For External Use Only

Flammable: Do not use near heat, flame, or while smoking

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age unless directed by a doctor

OTC - WHEN USING SECTION

When using this product

Avoid contact with eyes

Use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

Contents under pressure.

Do not puncture or incinerate. Do not store at temperature above 120°C F (49°C).

OTC - STOP USE SECTION

Stop use and ask doctor if

Irritation occurs

There is no improvement within 4 weeks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222)

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 socks at least once daily

Use daily for 4 weeks: if condition persists longer, ask 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 SAFETY INFORMATION

Store between 20°C to 25 °C (68° to 77°F)

INACTIVE INGREDIENT SECTION

Butylated Hydroxytoluene, Isobutane, polyethylene Glycol 400, Polysorbate 20, SD Alcohol 40B (32%)

OTC - QUESTIONS SECTION

1-800-925-4733

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313421tolnaftate 1 % Topical SprayPSN5
313421tolnaftate 10 MG/ML Topical SpraySCD5
313421tolnaftate 1 % Topical SpraySY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0155-05Walgreens Athletes Foot150 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY1505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0155WALGREENS ATHLETES FOOT (TOLNAFTATE SPRAY) AEROSOL, SPRAY [WALGREENS]5Current NDC, Legacy NDC, 1 package rows20241213_c68ad65d-b016-0069-e053-2995a90ae7ef.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-01550363-0155-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
Walgreens Athletes FootTOLNAFTATE SPRAYWalgreensc68ad65d-b016-0069-e053-2995a90ae7ef2024-12-11WarningsExact identifier
ndc (package): 0363-0155-05
ndc (product): 0363-0155
ndc11 (package): 00363015505
spl id: 28f10ac8-a7fa-c5e4-e063-6294a90a2eee
spl set id: c68ad65d-b016-0069-e053-2995a90ae7ef

Reported adverse events (FAERS/openFDA)#

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