Tinactin Deodorant Powder Spray Talc Free

Manufacturer: Bayer HealthCare LLC.
Effective date: 2025-12-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:19:40

Label at a glance#

ProductTinactin Deodorant

Active ingredientTOLNAFTATE

Label structure10 sections

Indications and uses

proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis) helps prevent most athlete's foot with daily use for effective relief of itching, burning and cracking

Dosage and administration

wash the 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 condition persists longer, ask a doctor to prevent athlete's ...

Storage and handling

store between 20° to 25°C (68° to 77° F)

Contacts and useful links#

PhoneLabel contact1-866-360-3266

Websitewww.tinactin.com

www.tinactin.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

(To Deliver) Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis)
helps prevent most athlete's foot with daily use
for effective relief of itching, burning and cracking

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Flammable:Do not use near heat, flame, or while smoking

Do not use on children under 2 years of age unless directed by a doctor

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes
use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
contents under pressure. do not puncture or incinerate. Do not store at temperatures above 120°F.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation occurs
there is no improvement within 4 weeks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash the 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 condition persists longer, ask a doctor
to prevent athlete's foot, apply once or twice daily (morning and/or night)
this product is not effective on the scalp or nails

Other information

STORAGE AND HANDLING SECTION

store between 20° to 25°C (68° to 77° F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

butylated Hydroxytoluene, fragrance, hydroxypropyl cellulose, isobutane, kaolin, magnesium stearate, PPG-12-Buteth-16, SD Alcohol 40-B (9% v/v),zea mays (corn) starch

Questions?

OTC - QUESTIONS SECTION

1-866-360-3266 or visit us at www.tinactin.com

PRINCIPAL DISPLAY PANEL - 133 g Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOUGH ACTIN' _®

Tinactin _®

tolnaftate ANTIFUNGAL

CURES AND PREVENTS

MOST ATHLETE'S FOOT

Relieves:

Itching
Burning

DEODORANT
POWDER SPRAY

Fights Odor

Talc Free

NET WT 133g (4.6 oz) PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
705936	Tinactin 1 % Powder Spray	PSN	2
705934	tolnaftate 1 % Powder Spray	PSN	2
705936	tolnaftate 0.01 MG/MG Powder Spray [Tinactin]	SBD	2
705934	tolnaftate 0.01 MG/MG Powder Spray	SCD	2
705936	Tinactin 0.01 MG/MG Powder Spray	SY	2
705936	Tinactin 1 % Powder Spray	SY	2
705934	tolnaftate 1 % Powder Spray	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11523-0137-1	TinactinDeodorant	133 g in 1 CAN	AEROSOL, POWDER	133		2

Products#

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

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

Tinactin Deodorant
Tolnaftate
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
KAOLIN
STARCH, CORN
BUTYLATED HYDROXYTOLUENE
ISOBUTANE
PPG-12-BUTETH-16
MAGNESIUM STEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11523-0137	11523-0137-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	IACT
KAOLIN	24H4NWX5CO	IACT
STARCH, CORN	O8232NY3SJ	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
ISOBUTANE	BXR49TP611	IACT
PPG-12-BUTETH-16	58CG7042J1	IACT
TOLNAFTATE	06KB629TKV	ACTIB
MAGNESIUM STEARATE	70097M6I30	IACT

Source Document#

Source XML

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
Tinactin Deodorant	TOLNAFTATE	Bayer HealthCare LLC.	1751d576-e94a-d7d1-e063-6294a90a03ff	2025-12-04	Warnings	Exact identifier ndc (package): 11523-0137-1 ndc (product): 11523-0137 ndc11 (package): 11523013701 spl id: 4526e2eb-ee89-3ac4-e063-6394a90a133f spl set id: 1751d576-e94a-d7d1-e063-6294a90a03ff

Reported adverse events (FAERS/openFDA)#

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