wart removal pen

Manufacturer
Wenchang Panzhijie Trading Co., Ltd.
Effective date
2023-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:24:45

Label at a glance#

Productwart removal pen
Active ingredientCHLORHEXIDINE ACETATE, SALICYLIC ACID
Label structure10 sections

Dosage and administration

1 . Wash the corns or warts with warm water 2 . Take out the inner plug from the bottle , install the brushinto the bottle cap. press the brush tightly and tighten theca on the bottle 3 . Dry the skin , then open the cap , dip the liquid with thebrush and apply it on the wart or com , after the liquid driesand forms to be a mask apply the liquid again . Apply it inthe day and night and twice in each time 4 . Apply...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

salicylic acid 0.5%

Chlorhexidine acetate 0.2%

Purpose

OTC - PURPOSE SECTION

wart remover

Use

INDICATIONS & USAGE SECTION

For the removal of common and plantar warts. The common wart is easily recognized by the rough " cauliflower like'appearance on the surface. The plantar wart is recognized by its location only on the bottom of the foot, itstenderness, and theinterruption of the footprint pattern.

Warnings

WARNINGS SECTION

For external use only. Do not use on irritated skinor on any area that is infected or reddened. Do not use onmoles, birthmarks, warts with hairs growing from them, genitalwarts or warts on the face of mucous membranes. Ask a doctorbefore you use if you have diabetes or poor blood circulation When using this productavoid contact with eyes. If product getsinto the eye, flush with water for 15 minutes . Avoid inhalingvapors Stop and ask a doctor if discomfort persists. Extremelyflammable. Keep away from fire and flame. Cap bottle tightlyand store at room temperature away fror heat, Keep out ofreach of children. If swallowed, get medical help or contactpoison Control Center right away

Do not use

OTC - DO NOT USE SECTION

1 . On damaged skin ( cuts , abrasions , eczema , sunburn)

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

3 . If you are pregnant or breastfeeding

STOP USE AND SEE A DOCTOR

OTC - STOP USE SECTION

STOP USE AND SEE A DOCTOR IF

You become pregnant , or are planning to becomepregnant , while using the product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away freheat , Keep out ofreach of children . If swallowed , get medical help orcontactpoison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1 . Wash the corns or warts with warm water

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

3 . Dry the skin , then open the cap , dip the liquid with thebrush and apply it on the wart or com , after the liquid driesand forms to be a mask apply the liquid again . Apply it inthe day and night and twice in each time

4 . Applying it for 2 weeks until the skin recovers to ahealthy situation .

NOTICE : " lif warts or com are big , you should use it for a longer time . if swallowed , get medical help or contact a poison controlcenter right away

Inactive ingredients

INACTIVE INGREDIENT SECTION

water , frutus cnidii , kuh-seng , purslane , the rhizome of large-headed atractylodes , radix angelicae , Peak room , pericarpium citri reticulatae, asarum , fructus forsythiae , burdock , Bamboo leaf , Platycodon grandiflorum , Mint , the root bark of the peony tree , Radix Arnebiae seu lithosperm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83717-001-0183717-001-01

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83717-00183717-001-01, 83717-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
0741156b-a594-74c8-e063-6394a90af4340717a8f7-7f56-0309-e063-6294a90a3ffb2023-10-08WarningsExact identifier
spl id: 0741156b-a594-74c8-e063-6394a90af434
spl set id: 0717a8f7-7f56-0309-e063-6294a90a3ffb

Reported adverse events (FAERS/openFDA)#

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