LXHUKU WART REMOVER

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:51:31

Label at a glance#

ProductLXHUKU WART REMOVER
Active ingredientSALICYLIC ACID
Label structure13 sections

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%

Purpose

OTC - PURPOSE SECTION

Wart Remover

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

hard paraffin,lanolin,phenol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1717

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603692747GTIN-13: 6974603692747
EAN-13: 6974603692747
GTIN storage (14 digits): 06974603692747
3a8754c3cf8d45728d3726fa1ecc4527.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-24684010-246-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOL339NCG44TVIACT
SALICYLIC ACIDO414PZ4LPZACTIB
PARAFFINI9O0E3H2ZEIACT
LANOLIN7EV65EAW6HIACT

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
4a3a0758-4d22-7dda-e063-6394a90a93bf47dc7d95-2527-488e-e063-6294a90a733a2026-02-07WarningsExact identifier
spl set id: 47dc7d95-2527-488e-e063-6294a90a733a

Reported adverse events (FAERS/openFDA)#

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