IZKUT Fungal Nail Patches

Manufacturer
Shenzhen Situya Trading Co., Ltd.
Effective date
2024-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:04

Label at a glance#

ProductIZKUT Fungal Nail Patches
Active ingredientTOLNAFTATE
Label structure14 sections

Dosage and administration

■ Clean and thoroughly dry the affected area before application. ■ Peel off the patch's protective film, starting with the outer side and then the inner side. ■ Place the sticky side of the patch directly onto the infected area on the nail and remove the release paper. ■ Gently wrap the sides of the toe or finger to ensure a snug fit. ■ Fold the remaining adhesive part to cover the toe/fingertip. ■ Leave the patch...

Storage and handling

■ Store at room temperature and keep away from direct sunlight. ■ Skin discoloration may occur during or after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Anti-Fungal

Use

INDICATIONS & USAGE SECTION

Repairs fungal nail damage and improves nail appearance

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

■ Do not use if you are allergic to any of the ingredients
■ Do not use if you are pregnant or breastfeeding

When Using

OTC - WHEN USING SECTION

■ Avoid direct contact with eyes, mouth, mucous membrane, wounds

Stop Use

OTC - STOP USE SECTION

■ if irritation occurs and discomfort persists

Ask Doctor

OTC - ASK DOCTOR SECTION

■ if you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ In case of contact with eyes, flush with water for at least 15 minutes.
■ If swallowed, seek medical assistance immediately or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Clean and thoroughly dry the affected area before application.
■ Peel off the patch's protective film, starting with the outer side and then the inner side.
■ Place the sticky side of the patch directly onto the infected area on the nail and remove the release paper.
■ Gently wrap the sides of the toe or finger to ensure a snug fit.
■ Fold the remaining adhesive part to cover the toe/fingertip.
■ Leave the patch on for 6–8 hours (It is recommended to use overnight for 3–6 months).

Other information

STORAGE AND HANDLING SECTION

■ Store at room temperature and keep away from direct sunlight.
■ Skin discoloration may occur during or after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Water

Questions

OTC - QUESTIONS SECTION

IZKUT LLC
5830 E 2ND ST, STE 7000 #5472
CASPER, WY 82609
Call: 1-307-247-9088
Email: service@izkutllc.com
Website: www.izkutllc.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82739-022IZKUT FUNGAL NAIL PATCHES (FUNGAL NAIL PATCHES) PATCH [SHENZHEN SITUYA TRADING CO., LTD.]1Unmatched20240823_203e15ab-9111-cd73-e063-6294a90a81b4.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82739-02282739-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TOLNAFTATE06KB629TKVACTIB
GLYCERINPDC6A3C0OXIACT

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
3a8415dc-b07b-3934-e063-6394a90a4f31203e15ab-9111-cd73-e063-6294a90a81b42025-07-22WarningsExact identifier
spl set id: 203e15ab-9111-cd73-e063-6294a90a81b4

Reported adverse events (FAERS/openFDA)#

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