FUNGAL NAIL TREATMENT

Manufacturer
Shenzhen Yuetai Electronic Commerce Co., Ltd
Effective date
2024-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:02:43

Label at a glance#

ProductFUNGAL NAIL TREATMENT
Active ingredientSALICYLIC ACID, CHLORHEXIDINE ACETATE
Label structure12 sections

Dosage and administration

1.Before use, clean the affected area with soap and soak the nail in warm water to soften it. 2.For toenail fungus, scrape the dirt off the nail and g ently file the thickened part of the fungal nail until it's flat (be careful not to damage the nail bed). 3.You can use a nail file every 2-3 days to polish the surface of the affected area by applying a thin layer of liquid to the affected area, the skin under the ...

Storage and handling

Store in a cool, shaded place away from direct sunlight. Store at room temperature between 15-30°C (59-86°F).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID 2%

Chlorhexidine di(acetate) 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

Effectively treats nail fungus, discolouration, spliting,
thickening, crumbling and brittleness.

Warnings

WARNINGS SECTION

For external use only, do not ingest.

Do not use

OTC - DO NOT USE SECTION

Do not use on pregnant women or children under 2 years of age unless otherwise advised by a doctor.

OTC - WHEN USING SECTION

Avoid contact with eyes when using this product,if contact occurs rinse thoroughly with water.

If irritation occurs, discontinue use and consult a physician.If swallowed, call a poison control

centre or seek medical attention immediately. Exercise caution when using on severely ulcerated

skin.

OTC - STOP USE SECTION

Stop and aska doctor if discomfort persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children.If swallowed, get medical help or contact PoisonControl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Before use, clean the affected area with soap and soak the nail in warm water to soften it.
2.For toenail fungus, scrape the dirt off the nail and g ently file the thickened part of the fungal nail until
it's flat (be careful not to damage the nail bed).
3.You can use a nail file every 2-3 days to polish the surface of the affected area by applying a thin layer
of liquid to the affected area, the skin under the nail and around the cuticle.
4.Use twice daily, morning and evening.
5.Repeat this process 2-3 times a day until a healthy nail begins its gradual degeneration. For best results,
continue use for a continuous period of 6 weeks.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, shaded place away from direct
sunlight. Store at room temperature between
15-30°C (59-86°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Sorbitol,Alcohol,Propylene Glycol,Angelica
Dahurica,L aurocapram,Caramel,Dimethylol Urea,
Sunset Yellow

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84291-00284291-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
2e16bfed-6c41-04dd-e063-6294a90a98f7186b55f9-cbb4-e02d-e063-6294a90aac842025-02-14WarningsExact identifier
spl set id: 186b55f9-cbb4-e02d-e063-6294a90aac84

Reported adverse events (FAERS/openFDA)#

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