Tinactin Jock Itch 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 Jock Itch

Active ingredientTOLNAFTATE

Label structure10 sections

Indications and uses

cures most jock itch for effective relief of itching, chafing and burning

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

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 ingredient

OTC - ACTIVE INGREDIENT SECTION

(To Deliver) Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

cures most jock itch
for effective relief of itching, chafing and burning

Warnings

WARNINGS SECTION

OTC - DO NOT USE SECTION

For external use only

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

OTC - DO NOT USE SECTION

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 contents can be harmful or fatal
contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation occurs
there is no improvement within 2 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 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
use daily for 2 weeks; if condition persists longer, ask a doctor
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, hydroxypropyl cellulose, isobutane, kaolin, magnesium stearate, PPG-12-buteth-16, SD alcohol 40-B (9% w/w), zea mays (corn) starch

Questions?

OTC - QUESTIONS SECTION

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

PRINCIPAL DISPLAY PANEL - 133g Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOUGH ACTIN'_®

Tinactin_®

tolnaftate ANTIFUNGAL

Cures Most Jock Itch

Relieves:

Itching
Burning

POWDER SPRAY
Goes On Dry

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
11523-0138-1	TinactinJock Itch	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 Jock Itch
Tolnaftate
BUTYLATED HYDROXYTOLUENE
ISOBUTANE
PPG-12-BUTETH-16
KAOLIN
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE, UNSPECIFIED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11523-0138	11523-0138-1

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
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
ISOBUTANE	BXR49TP611	IACT
PPG-12-BUTETH-16	58CG7042J1	IACT
KAOLIN	24H4NWX5CO	IACT
TOLNAFTATE	06KB629TKV	ACTIB
MAGNESIUM STEARATE	70097M6I30	IACT
STARCH, CORN	O8232NY3SJ	IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	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 Jock Itch	TOLNAFTATE	Bayer HealthCare LLC	163ab4df-6e4a-6239-e063-6294a90a1cd0	2025-12-04	Warnings	Exact identifier ndc (package): 11523-0138-1 ndc (product): 11523-0138 ndc11 (package): 11523013801 spl id: 4526e2eb-ee8a-3ac4-e063-6394a90a133f spl set id: 163ab4df-6e4a-6239-e063-6294a90a1cd0

Reported adverse events (FAERS/openFDA)#

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