LXHUKU WART REMOVER- salicylic acid 17% wart remover patch

LXHUKU WART REMOVER by

Drug Labeling and Warnings

LXHUKU WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 17%

Purpose

Wart Remover

Use

For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface

Warnings

For external use only.

Do not use

On irritated,infected, or reddened skin; on genital warts and warts on the face; on moles, birthmarks, and warts with hair growing from them;on mucous mempranes.

When Using

Ask a doctor before use if you have diabetes or poor blood circulation

Stop Use

Ask a doctor before use if you have diabetes or poor blood circulation

Ask Doctor

Ask a doctor before use if you have diabetes poor blood circulation

Keep Oot Of Reach Of Children

If swallowed, get medical help or contact a Poison control Center right away.

Directions

wash affected area: may soak wart in warm water for 5 minutes dry area thoroughly,remove bandage strips by peeling backing off If necessary,cut medicated patch to fit wart carefully apply medicated plaster, repeat procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

Store between 59°and 86°F(15°and 30°C).

Inactive ingredients

hard paraffin,lanolin,phenol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LXHUKU WART REMOVER 
salicylic acid 17% wart remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-022-01	180 in 1 BOX; Type 0: Not a Combination Product	01/29/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	01/29/2026

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