WART REMOVER PATCHS

Manufacturer
Gaozhou Chapin Technology Co., Ltd
Effective date
2024-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:08

Label at a glance#

ProductWART REMOVER PATCHS
Active ingredientSALICYLIC ACID
Label structure12 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 week

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 20%

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

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 right away

DIRECTIONS

INSTRUCTIONS FOR USE 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 week

WHEN USING

OTC - WHEN USING SECTION

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

OTHER INFORMATION

WARNINGS AND PRECAUTIONS SECTION

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Ethylhexyl Acrylate ·Polyethylene Terephthalate

DOSAGE & ADMINISTRATION SECTION

One patch per day, each patch contains1 mg of tolnaftate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabellabellabellabellabellabellabellabellabellabellabellabellabellabellabellabellabel

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84168-015-112025-07-29C16284748780-13b156c62-2ec5-fb37-e063-e6dba90a4e071bb252dc-8f55-fb95-e063-6394a90a6a5f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84168-015-11WART REMOVER PATCHS16.8 g in 1 BOXPATCH16.81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84168-015WART REMOVER PATCHS (WART REMOVER) PATCH [GAOZHOU CHAPIN TECHNOLOGY CO., LTD]11 package rows20240626_1bb252dc-8f55-fb95-e063-6394a90a6a5f.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84168-01584168-015-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
1bb24de6-57c6-4a2c-e063-6394a90a17491bb252dc-8f55-fb95-e063-6394a90a6a5f2024-06-25WarningsExact identifier
spl id: 1bb24de6-57c6-4a2c-e063-6394a90a1749
spl set id: 1bb252dc-8f55-fb95-e063-6394a90a6a5f

Reported adverse events (FAERS/openFDA)#

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