85248-171update

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Effective date
2026-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-23 05:10:08

Label at a glance#

ProductKomxsum WART REMOVER PATCHES
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 1%

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 membranes

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

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 membranes

Ask Doctor

OTC - ASK DOCTOR SECTION

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

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

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843981484GTIN-13: 6979843981484
EAN-13: 6979843981484
GTIN storage (14 digits): 06979843981484
809121221179bfe86ddddb7a37cadb18.jpg

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
85248-17185248-171-01, 85248-171-02, 85248-171-03

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
SALICYLIC ACIDO414PZ4LPZACTIB
PARAFFINI9O0E3H2ZEIACT
PHENOL339NCG44TVIACT
LANOLIN7EV65EAW6HIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-03-24full-release2026-06-01 01:51:11

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
Komxsum WART REMOVER PATCHESSALICYLIC ACID 1% WART REMOVERJiangxi Yudexi Pharmaceutical Co., LTD4dc1da6f-661b-ae95-e063-6394a90aa4142026-07-20WarningsExact identifier
ndc (package): 85248-171-03
ndc (package): 85248-171-02
ndc (package): 85248-171-01
ndc (product): 85248-171
ndc11 (package): 85248017101
ndc11 (package): 85248017103
ndc11 (package): 85248017102
spl id: 571661df-3f0e-763c-e063-6394a90a4197
spl set id: 4dc1da6f-661b-ae95-e063-6394a90aa414

Reported adverse events (FAERS/openFDA)#

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