FDA.reportPublic FDA data

Albertsons - Signature Care Tolnaftate Liquid Spray

Manufacturer
Better Living Brands LLC
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:40:36

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) prevent recurrence of most athlete's foot with daily use for effective relief of 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, ...

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)
  • prevent recurrence of most athlete's foot with daily use
  • for effective relief of itching, burning and cracking

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 120ºF. Intentional misuse by delibrately 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 four weeks (for athlete's foot) or two weeks (for jock itch)

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

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, appl morning and/or night
  • this product is not effective on the scalp or nails
  • if nozzle clogs, clear under running water

​Other information

OTHER SAFETY INFORMATION

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

​Inactive ingredients

INACTIVE INGREDIENT SECTION

BHT, isobutane, PPG-12-buteth-16, SD alcohol 40-B

​Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antifungal

Athlete's Foot Liquid Spray

Tolnaftate 1%

  • Cures most athlete's foot & prevents recurrences
  • Relieves itching, cracking & burning

Net WT 5.3 OZ (150g)

ArtworkArtwork

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
21130-213-00Tolnaftate150 g in 1 CANISTERAEROSOL, SPRAY1505

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
21130-21321130-213-00

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
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ISOBUTANEBXR49TP611IACT
PPG-12-BUTETH-1658CG7042J1IACT
ALCOHOL3K9958V90MIACT
TOLNAFTATE06KB629TKVACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-07full-release2026-06-01 00:36:14

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 SPRAYBetter Living Brands LLCccff4830-6d81-2a0d-e053-2a95a90a154c2025-10-24WarningsExact identifier
ndc (package): 21130-213-00
ndc (product): 21130-213
ndc11 (package): 21130021300
spl id: 41eeb7c0-0631-f613-e063-6394a90ab838
spl set id: ccff4830-6d81-2a0d-e053-2a95a90a154c

Reported adverse events (FAERS/openFDA)#

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