Quality Choice Tolnaftate Powder Spray Talc-Free

Manufacturer: Chain Drug Marketing Association
Effective date: 2026-06-09
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: daily-update
Hydrated at: 2026-06-11 05:11:15

Label at a glance#

ProductTolnafate

Active ingredientTOLNAFTATE

Label structure10 sections

Indications and uses

cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch ( tinea cruris) helps prevent most athlete's foot with daily use relieves itching, burning, cracking, and chafing associated with jock itch

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 to...

Contacts and useful links#

PhoneLabel contact1-866-964-0939

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), ringworm (tinea corporis) and jock itch ( tinea cruris)
helps prevent most athlete's foot with daily use
relieves itching, burning, cracking, and chafing associated with jock itch

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

there is no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch
irriration occurs

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; for jock itch, use daily for 2 weeks
if condition persists, consult a doctor
this product is not effective on the scalp or nails

Other information

OTHER SAFETY INFORMATION

store between 20º and 30ºC (68º and 86ºF)
if nozzle clogs, clean with a pin

Inactive ingredients

INACTIVE INGREDIENT SECTION

Isobutane, SD Alcohol 40-B, Kaolin, Zea Mays (Corn) Starch,BHT, PPG-12-Buteth-16

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QC Quality Choice

Athlete's

Foot

Powder

Spray

Tolnaftate 1% / Antifungal

Cures Most Athlete's Foot

& Prevents Recurrences

Comforts & Refreshes

Talc-Free

Relieves:

Itching

Burning

Cracking

NET WT.

4.6 OZ. (130 g)

carton

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Tolnafate
Tolnaftate Powder Spray
TOLNAFTATE
ZEA MAYS (CORN) STARCH
BHT
PPG-12-BUTETH-16
ISOBUTANE
KAOLIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83324-234	83324-234-46

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TOLNAFTATE	06KB629TKV	ACTIB
ZEA MAYS (CORN) STARCH	O8232NY3SJ	IACT
BHT	1P9D0Z171K	IACT
PPG-12-BUTETH-16	58CG7042J1	IACT
ISOBUTANE	BXR49TP611	IACT
KAOLIN	24H4NWX5CO	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2026-04-15	full-release	2026-06-01 01:53:51
2	2025-11-06	monthly-update	2026-06-03 17:38:46
1	2025-05-01	full-release	2026-06-01 01:00:17

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tolnafate	TOLNAFTATE POWDER SPRAY	Chain Drug Marketing Association	342affe8-0a4d-6fe6-e063-6394a90a8dad	2026-06-09	Warnings	Exact identifier ndc (package): 83324-234-46 ndc (product): 83324-234 ndc11 (package): 83324023446 spl id: 53d79bf7-0252-bcd8-e063-6294a90a1772 spl set id: 342affe8-0a4d-6fe6-e063-6394a90a8dad

Reported adverse events (FAERS/openFDA)#

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