HUIPOLII NAIL PFLASTER- tolnaftate 1% nail pflaster patch

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Tolnaftate l%

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 Out Of Reach Of Children

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

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

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

INGREDIENTS AND APPEARANCE

HUIPOLII NAIL PFLASTER 
tolnaftate 1% nail pflaster patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-206
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
POLYESTER-7 (UNII: 0841698D2F)
WATER (UNII: 059QF0KO0R)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
DICLORAN (UNII: F0BE9UC5J7)
ACRYLIC ACID (UNII: J94PBK7X8S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-206-01	32 in 1 BOX; Type 0: Not a Combination Product	05/08/2026
2	NDC: 85248-206-02	64 in 1 BOX; Type 0: Not a Combination Product	05/08/2026
3	NDC: 85248-206-03	96 in 1 BOX; Type 0: Not a Combination Product	05/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	05/08/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.		411295811	manufacture(85248-206)