AlJIEYO WART REMOVER

Manufacturer
Shenzhen Yikai Electronic Technology Co., Ltd.
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:51:02

Label at a glance#

ProductAlJIEYO WART REMOVER
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

● wash affected area and dry thoroughly apply tag patch after 24 hours. remove tag patch ● repeat procedure every 24 hours for up to 14 days for tags /warts removal and up to 12 weeks for warts, until the problem hascleared. ● may hot compress wart in warm water for 5 minutes to assist in removal

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 12%

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 roughcauliflower-like appearance of the surface

● the plantar wart is recognized by its location only on the bottom of the foot,its tenderness and the interruption of the footprint pattern

Warnings

WARNINGS SECTION

For external use only.
Keep this and all drugs out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Stop using this product and see your doctor if discomfort persists for more than 72 hours

Do not use

OTC - DO NOT USE SECTION

●on irritated skin or on any area that is infected or reddened

●on moles, birthmarks, warts with hair growing from them, warts on the face or mucous membranes

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please store this product out of the reach of childre

Directions

DOSAGE & ADMINISTRATION SECTION

● wash affected area and dry thoroughly apply tag patch after 24 hours. remove tag patch

● repeat procedure every 24 hours for up to 14 days for tags /warts removal and up to 12 weeks for warts, until the problem hascleared.

● may hot compress wart in warm water for 5 minutes to assist in removal

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cnidium monnieri, Podophyllum,Hawthorn, Stellera chamaejasm, Sophora flavescens, Earthy hibiscus bark, Honeysuckle

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334499101010.110.1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2670162salicylic acid 12 % Medicated PatchPSN2
2670162salicylic acid 0.12 MG/MG Medicated PatchSCD2
2670162salicylic acid 12 % Medicated PatchSY2

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83809-003-01AlJIEYO WART REMOVER180 in 1 BOXPATCH1802
83809-003-02AlJIEYO WART REMOVER540 in 1 BOXPATCH5402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83809-003ALJIEYO WART REMOVER PATCH [SHENZHEN YIKAI ELECTRONIC TECHNOLOGY CO., LTD.]22 package rows20250109_0aa6206e-ea19-3a7e-e063-6294a90aaa38.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83809-00383809-003-01, 83809-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
2b18783b-150b-75d0-e063-6394a90acfa40aa6206e-ea19-3a7e-e063-6294a90aaa382025-01-07WarningsExact identifier
spl id: 2b18783b-150b-75d0-e063-6394a90acfa4
spl set id: 0aa6206e-ea19-3a7e-e063-6294a90aaa38

Reported adverse events (FAERS/openFDA)#

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