Wart Corn Remover Cream

Manufacturer
Shanghai Yijing Medical Technology Co., Ltd.
Effective date
2025-07-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:06:37

Label at a glance#

ProductWart Corn Remover Cream
Active ingredientSALICYLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 5%

OTC - PURPOSE SECTION

Wart Remover

INDICATIONS & USAGE SECTION

For the removal of warts, including plantar warts, flat warts, common warts, corns and calluses.

WARNINGS SECTION

For external use only.
Keep away from fire and flame.

OTC - WHEN USING SECTION

When using, keep out of eyes, ears, mouth and any open hurt skin area. In case of contact with eyes thoroughly with water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

DOSAGE & ADMINISTRATION SECTION


Wash the area affected by wart,corn or callus in warm water for 5 minutes.
Dry area thoroughly.
Use pea size cream and apply on the affected area.
Repeat this procedure once or twice daily as needed (until the wart, corn or callus is removed)for up to4weeks.

INACTIVE INGREDIENT SECTION

WATER
MENTHOL, (+)-
TEA TREE OIL
PETROLATUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2548833salicylic acid 5 % Topical CreamPSN1
2548833salicylic acid 50 MG/ML Topical CreamSCD1
2548833salicylic acid 5 % Topical CreamSY1

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
85157-003-01Wart Corn Remover Cream30 g in 1 BOTTLECREAM301

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85157-00385157-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
394f840d-e416-9331-e063-6394a90af247394f840d-e415-9331-e063-6394a90af2472025-07-06WarningsExact identifier
spl id: 394f840d-e416-9331-e063-6394a90af247
spl set id: 394f840d-e415-9331-e063-6394a90af247

Reported adverse events (FAERS/openFDA)#

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