87786-013

Manufacturer
Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Effective date
2026-07-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-17 21:45:44

Label at a glance#

ProductNATURAL CURES 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 • Using the applicator, apply a small amount of the product to sufficiently cover each wart and let it dry • Use once or twice daily as needed until wart is removed • Wart removal may take up to 12 weeks • Children under 2 years old: ask a doctor

Storage and handling

• Store at 20-25 °C (68-77 °F) • Keep cap tightly closed; avoid contact with fabrics surfaces • Protect from freezing and excessive heat • Tamper evident: do not use if seal is broken or missing

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 and plantar warts.
• The common wart is easily recognized by the rough "cauliflower-like" appearance of the surface
• The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and interruption of footprint pattern

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

• On irritated skin or any area that is infected
• If you are diabetic or have poor blood circulation
• On birthmarks, moles, warts with hair growing from them, genital warts, warts on face, or warts on mucous membranes

When Using

OTC - WHEN USING SECTION

• Avoid contact with eyes and mucous membranes
• If burning, discomfort, or irritation occurs, stop use and ask doctor
• Cap bottle tightly after use
• Keep away from heat and flame

Stop Use

OTC - STOP USE SECTION

• Discomfort persists
• Excessive irritation occurs
• You do not see improvement within 12 weeks

Ask Doctor

OTC - ASK DOCTOR SECTION

• Discomfort persists
• Excessive irritation occurs
• You do not see improvement within 12 weeks

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• wash affected area (may soak wart in warm water for 5 minutes)
• Dry area thoroughly
• Using the applicator, apply a small amount of the product to sufficiently cover each wart and let it dry
• Use once or twice daily as needed until wart is removed
• Wart removal may take up to 12 weeks
• Children under 2 years old: ask a doctor

Other information

STORAGE AND HANDLING SECTION

• Store at 20-25 °C (68-77 °F)
• Keep cap tightly closed; avoid contact with fabrics surfaces
• Protect from freezing and excessive heat
• Tamper evident: do not use if seal is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Polyethylene Glycol, Borneol

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1717

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87786-01387786-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
NATURAL CURES WART REMOVERSALICYLIC ACID 17% WART REMOVERWenzhou Yuyuan Pharmaceutical Co., Ltd.5650ed83-2572-083b-e063-6294a90a5d692026-07-11WarningsExact identifier
ndc (package): 87786-013-01
ndc (product): 87786-013
ndc11 (package): 87786001301
spl id: 5650ed83-2573-083b-e063-6294a90a5d69
spl set id: 5650ed83-2572-083b-e063-6294a90a5d69

Reported adverse events (FAERS/openFDA)#

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