IZKUT Fungal Nail Patches by Shenzhen Situya Trading Co., Ltd. 82739-022 Complete

IZKUT Fungal Nail Patches by

Drug Labeling and Warnings

IZKUT Fungal Nail Patches by is a Otc medication manufactured, distributed, or labeled by Shenzhen Situya Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

IZKUT FUNGAL NAIL PATCHES- fungal nail patches patch 
Shenzhen Situya Trading Co., Ltd.

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82739-022 Complete

Active Ingredient

Tolnaftate 1%

Purpose

Anti-Fungal

Use

Repairs fungal nail damage and improves nail appearance

Warnings

For external use only.

Do not use

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

When Using

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

Stop Use

■ if irritation occurs and discomfort persists

Ask Doctor

■ if you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

■ 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

■ 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

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

Inactive ingredients

Glycerin, Water

Questions

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

1

IZKUT FUNGAL NAIL PATCHES 
fungal nail patches patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 82739-022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82739-022-0132 in 1 BOX; Type 0: Not a Combination Product08/22/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00508/22/202407/22/2025
Labeler - Shenzhen Situya Trading Co., Ltd. (706154255)
Establishment
NameAddressID/FEIBusiness Operations
Shenzhen Situya Trading Co., Ltd.706154255manufacture(82739-022) , label(82739-022)

Revised: 7/2025