Forticept Antifungal Foot Gel

Manufacturer
Lidan, Inc. | Cosco International, Inc.
Effective date
2025-03-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:57:45

Label at a glance#

ProductForticept Antifungal Foot Gel
Active ingredientCLOTRIMAZOLE
Label structure12 sections

Indications and uses

• Cures most athlete's foot, jock itch and ringworm • Relieves itching, burning, cracking, scaling and discomfort which accompany these conditions • Helps keep feet dry and free of fungal infection For the treatment of fungal infections caused by: Athlete's foot (tinea pedis), Jock itch (tinea cruris), and Ringworm (tinea corporis)

Dosage and administration

Adults and children 2 years of age and older: • wash affected area and dry thoroughly • apply a thin layer over affected area once or twice daily • 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 socks at least once daily • for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use...

Label contents#

Full prescribing information#

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient/Purpose

Clotrimazole - 1% (Antifungal)

Uses

OTC - Purpose Section

• Cures most athlete's foot, jock itch and ringworm
• Relieves itching, burning, cracking, scaling and discomfort which accompany these conditions
• Helps keep feet dry and free of fungal infection

INDICATIONS & USAGE SECTION

For the treatment of fungal infections caused by: Athlete's foot (tinea pedis), Jock itch (tinea cruris), and Ringworm (tinea corporis)

WARNINGS:

WARNINGS SECTION

For external use only!

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

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if:
• irritation occurs
• there is no improvement within 4 weeks (for athlete's foot or ringworm) or 2 weeks (for jock itch).

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older:
• wash affected area and dry thoroughly
• apply a thin layer over affected area once or twice daily
• 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 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 longer, ask a doctor

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Allantoin, Alpha Tocopherol, Benzethonium Chloride, Cetosearyl Alcohol, Aluminum Starch Octenylsuccinate, Ethylhexylglycerin, Hexamethyldisilazane, Isohexadecane, Lanolin, Paraffinum Liquidum, Peppermint Oil, Petrolatum, Phenoxyethanol, Polyhexanide, Polysorbate 80, Propylene Glycol, Shea Butter, Sodium Acrylate / Sodium Acryloyldimethyl Taurate Copolymer, Steareth-2, Steareth-21, Tea Tree Oil, Thymol,
Water

Other Information:

SPL UNCLASSIFIED SECTION

• To open: unscrew cap and remove the seal.
• Store between 68° - 77°F (20° - 25°C)

For Questions:

OTC - QUESTIONS SECTION

Please call: +1 212 709-8133
Lidan, Inc.
30 Wall Street, 8th Floor
New York, NY 10005
www.forticept.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3oz label3oz label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049535clotrimazole 1 % Topical GelPSN2
1049535clotrimazole 0.01 MG/MG Topical GelSCD2
1049535clotrimazole 1 % Topical GelSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CLOTRIMAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72127-0806-02025-03-25C16284748780-12cef2736-6675-d83d-e063-dadaa90ab31fForticept Antifungal Foot Gel
72127-0806-02025-01-30C16284748780-12cef2736-6675-d83d-e063-dadaa90ab31fForticept Antifungal Foot Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72127-0806-0Forticept Antifungal Foot Gel0.085 kg in 1 TUBEGEL0.0852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72127-0806FORTICEPT ANTIFUNGAL FOOT GEL (CLOTRIMAZOLE) GEL [LIDAN, INC.]2Current NDC, 1 package rows20250327_1b5851fc-ae73-4e54-bb62-3ff928628b97.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72127-080672127-0806-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Forticept Antifungal Foot GelCLOTRIMAZOLELidan, Inc.1b5851fc-ae73-4e54-bb62-3ff928628b972025-03-25WarningsExact identifier
ndc (package): 72127-0806-0
ndc (product): 72127-0806
ndc11 (package): 72127080600
spl id: ed6062d8-e888-413c-bd50-6c6ed86d8a19
spl set id: 1b5851fc-ae73-4e54-bb62-3ff928628b97

Reported adverse events (FAERS/openFDA)#

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