85248-206

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD | Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:32

Key Label Information#

Active Ingredients And Purpose

Active Ingredient

Tolnaftate l%

Purpose

Anti-Fungal

Uses

Use

Repairs fungal nail damage and improves nail appearance

Warnings

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

Directions And Dosage

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 onfor 6-8 hours (It is recommended to use overnight for 3-6 months).

Other Label Information

Other information

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

Inactive ingredients

Water, Polyester Spandex, Acrylate Copolymer, Tackifying Resin,Glycerin,Silicone Oil Paper

PRINCIPAL DISPLAY PANEL

Label Images#

ea912672178e1baedae755a3f4560985
ea912672178e1baedae755a3f4560985

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2677690tolnaftate 1 % Medicated PatchPSN1
2677690tolnaftate 0.01 MG/MG Medicated PatchSCD1
2677690tolnaftate 1 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85248-206-01HuiPoLii NAIL PFLASTER32 in 1 BOXPATCH321
85248-206-02HuiPoLii NAIL PFLASTER64 in 1 BOXPATCH641
85248-206-03HuiPoLii NAIL PFLASTER96 in 1 BOXPATCH961

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85248-20685248-206-01, 85248-206-02, 85248-206-03

Ingredients#

Complete SPL Sections#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate l%

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 Out 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. lf 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 onfor 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

Water, Polyester Spandex, Acrylate Copolymer, Tackifying Resin,Glycerin,Silicone Oil Paper

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Source Document#

Source XML