FDA.reportPublic FDA data

Athletes Foot

Manufacturer
Quantum, Inc. | Sun Deep Inc.
Effective date
2025-10-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:39:37

Label at a glance#

ProductAthletes Foot
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

Cures and prevents most Athlete's Foot. Relieves itching and burning.

Dosage and administration

Wash affected area and dry thoroughly. Apply a thin layer over affected area twice daily (morning and night). Pay special attention to spaces between the toes, wear well fitting shoes and change shoes and socks at least once daily.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1.0%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

Cures and prevents most Athlete's Foot. Relieves itching and burning.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes. Stop and ask doctor if irritation occurs or there is no improvement within four weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not use on children under two years old unless under supervision of a doctor. If swallowed, seek medical help or contact the poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash affected area and dry thoroughly. Apply a thin layer over affected area twice daily (morning and night). Pay special attention to spaces between the toes, wear well fitting shoes and change shoes and socks at least once daily.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Achillea Millefolium (Yarrow) Extract, Allantoin, Anthemis Nobilis (Chamomile) Extract, Bentonite, Citric Acid, Echinacea Purpurea Extract, Equisetum Arvense (Horsetail) Extract, Glycereth-7 Cocoate, Glycerin, Glycyrrhiza Glabra (Licorice Root) Extract, Hamamelis Virginiana (Witch Hazel) Extract, Hibiscus Syriacus (Althaea) Extract, Kaolin, Laminaria Digitata (Sea Kelp) Extract, Magnesium Aluminum Silicate, Melaleuca Alternifolia (Tea Tree) Oil, Melissa Officinalis (Balm Mint) Extract, Menthol, Methyl Paraben, Mixed Tocopherols (Vitamin E), Origanum Vulgare (Oregano) Oil, Panthenol, Propyl Paraben, Purified Water, Rosmarinus Officinalis (Rosemary) Extract, Salvia Officinalis (Sage) Extract, Stearic Acid, Thymus Vulgaris (Thyme) Extract, Tussilago Farfara (Coltsfoot) Extract, Zinc Oxide.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: QUANTUM, INC.
PO BOX 2791, EUGENE, OR 97402

PRINCIPAL DISPLAY PANEL - 21 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Quantum ®
HEALTH

Athlete's
Foot

Quick Drying
Antifungal Formula

WITH A UNIQUE BLEND
OF HERBS, ESSENTIAL OILS,
TOPICAL NUTRIENTS

STOPS ITCHING & BURNING
ELIMINATES ODOR
USE DAILY FOR PREVENTION

CURES & PREVENTS MOST
ATHLETE'S FOOT

Ointment

D E R M A

Net Wt 21g / .75 OZ

PRINCIPAL DISPLAY PANEL - 21 g Tube Carton
PRINCIPAL DISPLAY PANEL - 21 g Tube Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
103951tolnaftate 1 % Topical CreamPSN4
103951tolnaftate 10 MG/ML Topical CreamSCD4
103951tolnaftate 1 % Topical CreamSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70084-510-012025-01-30C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot
70084-510-012025-01-30C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot
70084-510-012023-02-13C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot
70084-510-012023-02-13C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot
70084-510-012021-01-29C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot
70084-510-012021-01-29C16284748780-1ba0f9c33-4dd5-a910-e053-dadaa90a0b85Athlete's Foot

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70084-510-01Athletes Foot21 g in 1 TUBECREAM214
70084-510-01Athletes Foot1 in 1 CARTONCREAM14

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70084-51070084-510-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
ECHINACEA PURPUREAQI7G114Y98IACT
TEA TREE OILVIF565UC2GIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
TOCOPHEROLR0ZB2556P8IACT
WATER059QF0KO0RIACT
ALLANTOIN344S277G0ZIACT
CHAMOMILEFGL3685T2XIACT
BENTONITEA3N5ZCN45CIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EQUISETUM ARVENSE TOP1DP6Y6B65ZIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
GLYCERINPDC6A3C0OXIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
HIBISCUS SYRIACUS BARKU6PQI719P3IACT
HAMAMELIS VIRGINIANA TOPUDA30A2JJYIACT
KAOLIN24H4NWX5COIACT
LAMINARIA DIGITATA15E7C67EE8IACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
MELISSA OFFICINALISYF70189L0NIACT
METHYLPARABENA2I8C7HI9TIACT
OREGANO LEAF OIL7D0CGR40U1IACT
PANTHENOLWV9CM0O67ZIACT
PROPYLPARABENZ8IX2SC1OHIACT
ROSEMARYIJ67X351P9IACT
SAGE065C5D077JIACT
STEARIC ACID4ELV7Z65APIACT
THYMECW657OBU4NIACT
TUSSILAGO FARFARA FLOWERUEE27X2Q2MIACT
ZINC OXIDESOI2LOH54ZIACT
TOLNAFTATE06KB629TKVACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32023-02-06full-release2026-05-31 23:54:02

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
Athletes FootTOLNAFTATEQuantum, Inc.6cb95707-9831-41f1-a23e-9e3356141fdc2025-10-20WarningsExact identifier
ndc (package): 70084-510-01
ndc (product): 70084-510
ndc11 (package): 70084051001
spl id: 419d881a-db12-b5bd-e063-6294a90a0ea4
spl set id: 6cb95707-9831-41f1-a23e-9e3356141fdc

Reported adverse events (FAERS/openFDA)#

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