FDA.reportPublic FDA data

HEB Foot Odor Control Powder Spray

Manufacturer
HEB
Effective date
2025-11-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:42:06

Label at a glance#

ProductTolnaftate
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

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

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 conditions persist, consult a doctor to prevent athlete's foot, ap...

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

​Purpose

OTC - PURPOSE SECTION

Antifungal

​Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

​For external use only.

​Flammable:

SAFE HANDLING WARNING SECTION

Keep away from heat, sparks and open flame. Contents under pressure. Do not puncture or incinerate.  Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

​When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes or mouth

​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 conditions persist, consult a doctor
  • to prevent athlete's foot, apply once or twice daily (morning and/or night)
  • in case of clogging, clear nozzle under running water

​Other information

OTHER SAFETY INFORMATION

store between 20º and 30ºC (68ºF and 86º)

​Inactive ingredients

INACTIVE INGREDIENT SECTION

disteardimonium hectorite, fragrance, isobutane, isopropyl myristate, SD alcohol 40-B, sodium bicarbonate

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB

Foot Odor Control

Tolnaftate 1%

Antifungal Powder Spray

  • Reduces Foot Odor
  • Cures Most Athlete's Foot

NET WT 4 OZ (113g)

H-E-B_Foot Odor Control Spray_50-023HE.jpgH-E-B_Foot Odor Control Spray_50-023HE.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
705934tolnaftate 1 % Powder SprayPSN7
705934tolnaftate 0.01 MG/MG Powder SpraySCD7
705934tolnaftate 1 % Powder SpraySY7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-514-40Tolnaftate113 g in 1 CANAEROSOL, SPRAY1137

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
37808-51437808-514-40

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
62024-12-11full-release2026-06-01 00:42:33

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
TolnaftateFOOT ODOR CONTROL SPRAYHEBc585605b-ecb8-4dd8-9205-a9be02d751fa2025-11-03WarningsExact identifier
ndc (package): 37808-514-40
ndc (product): 37808-514
ndc11 (package): 37808051440
spl id: 42b86eda-83cf-5418-e063-6294a90ae383
spl set id: c585605b-ecb8-4dd8-9205-a9be02d751fa

Reported adverse events (FAERS/openFDA)#

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