FUNGAL NAIL PATCHES

Manufacturer
Shenzhen Yikai Electronic Technology Co., Ltd.
Effective date
2024-05-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:02:26

Label at a glance#

ProductFUNGAL NAIL PATCHES
Active ingredientTOLNAFTATE
Label structure9 sections

Dosage and administration

Please wipe your skin clean before use and apply it gently to the affected area.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Anti-fungal

Use

INDICATIONS & USAGE SECTION

1.Remove any nail polish before use.Wash nails and surrounding skin and dry thoroughly as oils and moisture reduce adhesion.
2.Tear off the protective paper of the patch and apply the patch to the need area of the nail.
3 Firmly cover the side of the toes or fingers with the patch.then fold the remaining adhesive part to completely cover the toes fingers tips.
4.The duration of application is 6-8 hours.(lt is recommended to use it before going to bed for 3-6 consecutive months to achieve the desired effect.

Warnings

WARNINGS SECTION

1. For external use only. Store in a cool and dry place.
2. If skin becomes red and swollen, or if burning, aching and other forms of irritation occur, cease using and seek medical advice at once.
3. It is normal to find bubbles in the colloid.
4. Keep out of reach of children.

Stop Use

OTC - STOP USE SECTION

This product has not been found allergic. If allergic occurs, stop using it immediately.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please store this product out of the reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Please wipe your skin clean before use and apply it gently to the affected area.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Lonicerae Japonicae flos,Angelicae,Glycerin, Allantoin, Garlic Extract, Tea Tree Oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Products#

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DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83809-01883809-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
18899d16-6c67-fda9-e063-6394a90a75460e7fdebd-8ab9-024a-e063-6394a90afec32024-05-15WarningsExact identifier
spl id: 18899d16-6c67-fda9-e063-6394a90a7546
spl set id: 0e7fdebd-8ab9-024a-e063-6394a90afec3

Reported adverse events (FAERS/openFDA)#

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