WART REMOVER 87298-053-01

Manufacturer
Guangzhou Hechuang Commercial Service Co.,Ltd.
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-21 02:01:37

Label at a glance#

ProductWART REMOVER
Active ingredientSALICYLIC ACID
Label structure12 sections

Indications and uses

• for the removal of common and plantar warts

Dosage and administration

Directions • Wash the affected area. • You may soak the wart in warm water for about 5 minutes. • Dry the area thoroughly. • Apply a small amount to sufficiently cover each wart using the precision brush or a dual-tip cotton swab. • Allow to dry completely. • Repeat once or twice daily as directed until the wart is removed, for up to 12 weeks.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%

Purpose

OTC - PURPOSE SECTION

Wart remover

Uses

INDICATIONS & USAGE SECTION

• for the removal of common and plantar warts

Warnings

WARNINGS SECTION

Warnings
• For external use only.
• Keep away from fire or flame.

Do not use
• on irritated, infected, or reddened skin
• on moles, birthmarks, warts with hair growing from them,or genital warts
• on warts on the face or mucous membranes
• if you have diabetes or poor blood circulation

When using this product
• avoid contact with eyes
• if product gets into the eyes, flush with water for 15 minutes
• avoid contact with surrounding healthy skin
• avoid inhaling vapors

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if
• excessive irritation occurs
• discomfort persists
• the condition worsens

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.
• You may soak the wart in warm water for about 5 minutes.
• Dry the area thoroughly.
• Apply a small amount to sufficiently cover each wart using the precision brush or a dual-tip cotton swab.
• Allow to dry completely.
• Repeat once or twice daily as directed until the wart is removed, for up to 12 weeks.

Other Information

OTHER SAFETY INFORMATION

• Cap bottle tightly after each use.
• Store at room temperature away from heat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Laurocapram, Nitrocellulose, Poliglusam,Polyvinyl Alcohol, Purified Water

DESCRIPTION SECTION

MAXIMUM STRENGTH

√ QUICK-DRY FILM
√ PRECISION BRUSH
√ TARGETED WART REMOVAL

INCLUDES 10 DUAL-TIP COTTON SWABS

QUICK-DRY FILM FORMULA
Designed for targeted removal of common and plantar warts.

PRECISION APPLICATION
Brush directly onto the wart for controlled application.

DRYING FILM

Dries to form a thin film over the treated area.


TWO WAYS TO APPLY
Precision Brush 10 Dual-Tip Cotton Swabs

TARGETED
EASY APPLICATION
LESS MESS

INCLUDES:
1 × 30 mL Wart Remover
10 × Dual-Tip Cotton Swabs
1 × Instruction Leaflet

Made in China

REMS ADMINISTRATIVE INFORMATION

Distributor: Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Address: The first room on the west side of Suite 510, Oushang Building, No. 1119 Ouhai Avenue, Louggiao Subdistrict, Ouhai District, Zhejiang 325600, China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87298-05387298-053-01

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.594ecfe5-8d9d-be3b-e063-6294a90a5f2e2026-08-18WarningsExact identifier
ndc (package): 87298-053-01
ndc (product): 87298-053
ndc11 (package): 87298005301
spl id: 594ecff8-95f2-e39f-e063-6394a90a4966
spl set id: 594ecfe5-8d9d-be3b-e063-6294a90a5f2e

Reported adverse events (FAERS/openFDA)#

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