Wart Remover

Manufacturer
Guangzhou Hechuang Commercial Service Co.,Ltd.
Effective date
2026-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-17 21:45:41

Label at a glance#

ProductWart Remover
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

Directions ●Wash the affected area ●Soak the wart in warm water for 5 minutes and dry it thoroughly Apply one drop at a time with the applicator to cover the skin tag completely ●Allow to dry, use self-adhesive cushioning pads to cover the wart if desired Repeat this process once or twice daily as needed, for up to 12 weeks, until the wart is removed (Note: For external use, and can not be applied to healthy skin)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 8%

Purpose

OTC - PURPOSE SECTION

Wart Remover

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Brucea Javanica Whole, Angelica Dahurica Root, Sophora Flavescens Root, Arnebia Euchroma Root, Phenoxyethanol

Use

INDICATIONS & USAGE SECTION

Uses for the removal corns, calluses, plantar warts, flat warts, common warts (less than 5 mm in size).

Warnings

WARNINGS SECTION

Warnings

●For external use only
●FLAMMABLE. Keep away from fire or flame.

When using this product
●keep out of eyes, ears, and mouth
●If product gets in eyes, flush with water for 15 minutes

Do not use
●If you have diabetes or poor blood circulation, please do not use.
●Do not use on irritated, infected or reddened skin; moles, birthmarks, hairy warts, genital warts, facial warts or any mucous membranes.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor
If discomfort persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
●Wash the affected area
●Soak the wart in warm water for 5 minutes and dry it thoroughly Apply one drop at a time with the applicator to cover the skin tag completely
●Allow to dry, use self-adhesive cushioning pads to cover the wart if desired Repeat this process once or twice daily as needed, for up to 12 weeks, until the wart is removed (Note: For external use, and can not be applied to healthy skin)

Other Information

OTHER SAFETY INFORMATION

Store between 20° to 25°C (68° to 77° F) and keep tightly closed

DESCRIPTION SECTION

√ CLINICALLY FORMULATED WART TREATMENT

√ TARGETS COMMON & PLANTAR WARTS

√ AT-HOME WART REMOVAL SOLUTION

REMS ADMINISTRATIVE INFORMATION

Manufacturer: Zhenping Renkang Industrial Co., Ltd.

Address: No,10 Xinxing Road,Zhenping Industrial Agglomeration Zone, China

MADE IN PRC

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANELPRINCIPAL DISPLAY PANEL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136977522572817GTIN-13: 6977522572817
EAN-13: 6977522572817
GTIN storage (14 digits): 06977522572817
Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87298-04787298-047-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
Wart RemoverSALICYLIC ACIDGuangzhou Hechuang Commercial Service Co.,Ltd.562a0178-1653-df26-e063-6394a90aa37f2026-07-09WarningsExact identifier
ndc (package): 87298-047-01
ndc (product): 87298-047
ndc11 (package): 87298004701
spl id: 562a14a4-1e61-60db-e063-6294a90aab1e
spl set id: 562a0178-1653-df26-e063-6394a90aa37f

Reported adverse events (FAERS/openFDA)#

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