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Tolnaftate

Generic Name
Tolnaftate
Brand Names
Absorbine Jr Antifungal, Clarus, Fungi-nail, Fungoid-D, Sanafitil Antifungal, Silka Cream, Tinactin, Tineacide Antifungal, Ting
Drug Type
Small Molecule
Chemical Formula
C19H17NOS
CAS Number
2398-96-1
Unique Ingredient Identifier
06KB629TKV

Overview

Tolnaftate is a synthetic over-the-counter anti-fungal agent. It may come as a cream, powder, spray, or liquid aerosol, and is used to treat jock itch, athlete's foot and ringworm. It is sold under several brand names, most notably Tinactin and Odor Eaters.

Indication

Tolnaftate topical is used to treat skin infections such as athlete's foot, jock itch, and ringworm infections. Tolnaftate is also used, along with other antifungals, to treat infections of the nails, scalp, palms, and soles of the feet. The powder and powder aerosol may be used to prevent athlete's foot.

Associated Conditions

  • Dermatophytosis
  • Pityriasis versicolor
  • Ringworm
  • Tinea Corporis
  • Tinea Cruris
  • Tinea Pedis

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-097
TOPICAL
1 g in 100 mL
4/14/2025
WinCo Foods LLC
67091-753
TOPICAL
10 mg in 1 mL
6/21/2025
ProPedix, Inc.
85565-002
TOPICAL
1 g in 100 g
5/20/2025
PURETEK CORPORATION
59088-443
TOPICAL
0.1 g in 10 mL
10/17/2023
Jiangxi Yudexi Pharmaceutical Co., LTD
85248-004
TOPICAL
1 g in 100 mL
4/22/2025
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-126
TOPICAL
1 g in 100 mL
5/26/2025
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-119
TOPICAL
1 g in 100 mL
5/23/2025
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-118
TOPICAL
1 g in 100 mL
5/23/2025
TAGRID LLC
85384-0010
TOPICAL
10 mg in 1 g
6/9/2025
PURETEK CORPORATION
59088-279
TOPICAL
10 mg in 1 g
3/14/2024

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
NAFTATE LOTION 1% w/v
SIN04429P
LOTION
1% w/v
5/21/1990
NAFTATE CREAM 1% w/w
SIN04473P
CREAM
1% w/w
5/21/1990

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
TINADERM tolnaftate 0.9 mg/g pressurised spray aerosol can
18221
Medicine
A
10/8/1991
Flexitol Medicated Anti-Fungal Cream
149955
Medicine
A
2/7/2008
TINADERM POWDER Bottle
18222
Medicine
A
10/8/1991

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
TINACTIN CHILL DEODORANT POWDER SPRAY
Bayer Inc
02319276
Powder ,  Aerosol - Topical
1 % / W/W
7/18/2009
ODOR-EATERS
blistex corporation
02244777
Aerosol - Topical
1 % / W/W
3/7/2002
ANTIFUNGAL TINCTURE
nsc pharma gmbh & co.kg
02475324
Tincture - Topical
1 % / W/W
N/A
ATHLETE'S FOOT CREAM
the avon company canada limited
02508788
Cream - Topical
1 % / W/W
N/A
TOLNAFTATE ANTIFUNGAL CREAM
g&w laboratories inc.
02244939
Cream - Topical
1 %
11/30/2005
TINACTIN PLUS POWDER 1%
schering-plough canada inc
01942581
Powder - Topical
1 %
12/31/1993
SNAP-STIKS SENIOR'S FOOT FUNGUS RELIEF SWABS WITH TOLNAFTATE
ams homecare inc.
02253305
Swab - Topical
1 %
N/A
TINACTIN JOCK ITCH CRM 10MG/GM
schering-plough canada inc
00614211
Cream - Topical
10 MG / G
12/31/1984
FOOTWORKS HEALTHY ANTIFUNGAL SPRAY FOR ATHLETE'S FOOT
the avon company canada limited
02375397
Spray - Topical
1 % / W/W
2/29/2012
FOOTLOGIX ANTI FUNGAL MOUSSE FORMULA
kvg group inc
02394448
Aerosol - Topical
1 % / W/W
N/A

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
SOLUFUNGIN 10 mg/ml SOLUCION CUTANEA
Arafarma Group S.A.
61933
SOLUCIÓN CUTÁNEA
Sin Receta
Not Commercialized
CUATROCREM CREMA
Galenicum Derma S.L.U.
51784
CREMA
Medicamento Sujeto A Prescripción Médica
Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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