DRMITSUI WART REMOVER

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2026-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:48:15

Label at a glance#

ProductDRMITSUI WART REMOVER
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS PURPOSE

Salicylic Acid 17%.--...Wart Remover

OTC - PURPOSE SECTION

FLAT WARTS

GENITAL WARTS

FILIFORM WARTS

COMMON WARTS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach children

WARNINGS SECTION

WARNINGS
For external use only.frammable. Keep away from

INDICATIONS & USAGE SECTION

For the removal of commonand plantar warts.The common wart is easilyrecognized by the rough"cauliflower-like” appearanceon the surface.The plantar wart is recognizedby its location only on thebottom of the footits tenderness,and the interruption of thefootprint pattern.Individuals seeking wartremoval, superficial skin wartgrowths, flat warts, filiformstoto genians

DOSAGE & ADMINISTRATION SECTION

Wash affected area.May soak wart in warm waterfor 5 minutes.

Dry area thoroughly.appureopateentdsufficiently cover each wart.

Let dry.oree hi arnecder oncwart is removed) for up to12 weeks.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS

Water, Carbomer, Glycerol,Triethanolamine, Ethyl Paraben.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN1
312881salicylic acid 170 MG/ML Topical SolutionSCD1
312881salicylic acid 17 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85593-118-01DRMITSUI WART REMOVER20 g in 1 BLISTER PACKLIQUID201

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-11885593-118-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
55a38b3a-a741-f0e9-e063-6294a90ac8854bf174a1-5369-4937-e063-6294a90a4bff2026-07-02WarningsExact identifier
spl set id: 4bf174a1-5369-4937-e063-6294a90a4bff

Reported adverse events (FAERS/openFDA)#

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