FDA.reportPublic FDA data

Target Antifungal Foot Odor Control Powder Spray

Manufacturer
Target Corporation
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:42:32

Label at a glance#

ProductTolnaftate
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

cures most athlete's foot (tinea pedis) and ringworm (tinea corporis) prevents the recurrence of most athlete's foot with daily use relieves itching, burning and cracking

Dosage and administration

wash affected area and dry thoroughly shake can well and spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night) supervise children in the use of this product for athlete's foot: pay special attention to spaces between the toe...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

​ ​Purpose

OTC - PURPOSE SECTION

Antifungal

​Uses

INDICATIONS & USAGE SECTION

  • cures most athlete's foot (tinea pedis) and ringworm (tinea corporis)
  • prevents the recurrence of most athlete's foot with daily use
  • relieves itching, burning and cracking

​Warnings

WARNINGS SECTION

​For external use only.

Extremely ​Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire, sparks and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.

Do not use

WARNINGS SECTION

on children under 2 years of age unless directed by a doctor.

​When using this product

OTC - WHEN USING SECTION

  • avoid spraying in eyes
  • use only as directed
  • intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

​Stop use and ask 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 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 of the product over affected area twice daily (morning and night) or as directed by a doctor
  • to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or 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
  • for athlete's foot and ringworm, use daily for 4 weeks
  • if conditions persist longer, consult a doctor
  • this product is not effective on the scalp or nails

​Other information

OTHER SAFETY INFORMATION

  • store between 20º and 30ºC (68ºF and 86º)
  • if nozzle clogs, clear under running warm water until unclogged

​Inactive ingredient

INACTIVE INGREDIENT SECTION

ISOBUTANE, SD ALCOHOL 40-B, ISOPROPYL MYRISTATE, SODIUM BICARBONATE, DISTEARDIMONIUM HECTORITE, FRAGRANCE,

​Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Odor -Eaters

Spray Powder

Antifungal

Foot Odor

Control

Powder

Spray

Tolnaftate 1% / Antifungal

  • Cures most athlete's foot

and prevents recurrences

  • Relieves itching, cracking

and burning

  • Reduces foot odor
  • Comforts and refreshes
  • Talc free

NET WT. 4 OZ. (113 g)

cartoncarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
705934tolnaftate 1 % Powder SprayPSN2
705934tolnaftate 0.01 MG/MG Powder SpraySCD2
705934tolnaftate 1 % Powder SpraySY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130034197005869GTIN-13: 0034197005869
EAN-13: 0034197005869
GTIN-12: 034197005869
UPC-A: 034197005869
GTIN storage (14 digits): 00034197005869		Target_upup_Foot Odor Control Spray_46-FSSTG-04.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-402-01Tolnaftate113 g in 1 CANAEROSOL, POWDER1132

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-40282442-402-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ISOBUTANEBXR49TP611IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALCOHOL3K9958V90MIACT
SODIUM BICARBONATE8MDF5V39QOIACT
TOLNAFTATE06KB629TKVACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-06-10full-release2026-06-01 01:03:03

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 POWDER SPRAY WITH BAKING SODATarget Corporation37792b12-c3dc-558f-e063-6294a90a7e752025-11-06WarningsExact identifier
ndc (package): 82442-402-01
ndc (product): 82442-402
ndc11 (package): 82442040201
spl id: 42f403bf-8d23-373c-e063-6394a90a203d
spl set id: 37792b12-c3dc-558f-e063-6294a90a7e75

Reported adverse events (FAERS/openFDA)#

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