Toenail Fungus Treatment

Manufacturer
Shenzhen Wankelai E-commerce Co., Ltd.
Effective date
2026-03-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:51:11

Label at a glance#

ProductToenail Fungus Treatment
Active ingredientTERBINAFINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Terbinafine 1%

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

For the effective treatment of nail fungus, discoloration, thickening, splitting,
crumbling and brittleness.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

If on children under 2 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

·Avoid contact with eyes.

OTC - STOP USE SECTION

Irritation occurs or if there is no improvement within 4 weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION


Apply the product twice a day, in the morning and at night.
Soak nails in warm water to soften, then gently file affected nails.
Clean the affected area with soap and water and dry thoroughly.
Directly to affected nail
Allow a few minutes to dry after each.
Use daily for 4-6 weeks, depending on the condition of the area needing repair.

INACTIVE INGREDIENT SECTION

ALCOHOL,DIMETHICONE,CETOSTEARYL ALCOHOL,TEA TREE OIL,PROPYLENE GLYCOL,TOCOPHEROL,SAFFLOWER OIL,WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
992531terbinafine HCl 1 % Topical SolutionPSN1
992531terbinafine hydrochloride 10 MG/ML Topical SolutionSCD1
992531terbinafine hydrochloride 1 % Topical SolutionSY1

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR Codesupport@antifung.comlabel.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
55a24767-1759-5f6a-8888-ea4aa0adac21Product name120140508
db9701af-cb4f-b8ba-d282-6bc5b6b7c467Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87413-002-01Toenail Fungus Treatment10 mL in 1 BOTTLELIQUID101

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87413-00287413-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Toenail Fungus TreatmentTERBINAFINEShenzhen Wankelai E-commerce Co., Ltd.4dc1d7f7-e4ae-c54b-e063-6394a90aa4202026-03-24WarningsExact identifier
ndc (package): 87413-002-01
ndc (product): 87413-002
ndc11 (package): 87413000201
spl id: 4dc1d7f7-e4af-c54b-e063-6394a90aa420
spl set id: 4dc1d7f7-e4ae-c54b-e063-6394a90aa420

Reported adverse events (FAERS/openFDA)#

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