Wart removal

Manufacturer
Wenchang Panzhijie Trading Co., Ltd.
Effective date
2023-11-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:02:27

Label at a glance#

ProductWart removal
Active ingredientSALICYLIC ACID, CHLORHEXIDINE ACETATE
Label structure10 sections

Dosage and administration

1 . Wash the coms or warts with wam water 2 . Take out the inner plug from the bottle , install thebrush into the bottle cap . press the brush tightly , and tighten the cap on the bottle 3 . Dry the skin , then open the cap , dip the brush into thethe liquid with the brush and apply it to the wart or com .after the liquid dnes and forms a mask , apply the liquid again Apply t in the day and night , and twice in ea...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

salicylic acid 0.3%

Chlorhexidine acetate 0.3%

Purpose

OTC - PURPOSE SECTION

wart remover

Use

INDICATIONS & USAGE SECTION

To remove warts such as plantar wart , flat wart commonwart and coms calluses

Warnings

WARNINGS SECTION

For extemal use only , do not get in eyes or swallow. Children should use it under the supervision of adults.

Keep out of reach of children

The liquid can easily volatilize & crystallize tighten thecap after use

Avoid prolonged contact with air during use

Do not use

OTC - DO NOT USE SECTION

On damaged skin ( cuts , abrasionseczema , sunburn)

If you are allergic to any of the ingredients in this product .

If you are pregnant or breastfeeding

STOP USE AND SEE A DOCTOR

OTC - STOP USE SECTION

STOP USE AND SEE A DOCTOR IF

if discomfort persists

if you have diabetes or poor blood circulation

Keep out of reach of children . If swallowed , get medical help or contact a Poison Control Center( 1-800-222-1222 ) nght away .

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( 1-800-222-1222 ) nght away .

Directions

DOSAGE & ADMINISTRATION SECTION

1 . Wash the coms or warts with wam water

2 . Take out the inner plug from the bottle , install thebrush into the bottle cap . press the brush tightly , and tighten the cap on the bottle

3 . Dry the skin , then open the cap , dip the brush into thethe liquid with the brush and apply it to the wart or com .after the liquid dnes and forms a mask , apply the liquid again Apply t in the day and night , and twice in each time

4 . Use t for 2 weeks untl the skin to a healthy situation

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, purslane , the rhizome of large-headed atractylodes, radix angelicae , pericarpium citri reticulata, Bamboo leaf , Platycodon grandiflorum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83717-002-0183717-002-01

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORHEXIDINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83717-002-012025-01-30C16284748780-12cef2736-a79f-d83d-e063-dadaa90ab31f83717-002

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83717-002-01Wart removal15 mL in 1 BOXLIQUID153

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83717-002WART REMOVAL (WART REMOVAL LIQUID) LIQUID [WENCHANG PANZHIJIE TRADING CO., LTD.]31 package rows20231119_071b08ac-fbd9-2854-e063-6294a90afd3e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83717-00283717-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
0a518fbe-7dec-d815-e063-6294a90ac79c071b08ac-fbd9-2854-e063-6294a90afd3e2023-11-16WarningsExact identifier
spl id: 0a518fbe-7dec-d815-e063-6294a90ac79c
spl set id: 071b08ac-fbd9-2854-e063-6294a90afd3e

Reported adverse events (FAERS/openFDA)#

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