Samsali Wart Corn Remover Pads

Manufacturer
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Effective date
2024-09-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:19:46

Label at a glance#

ProductSamsali Wart Corn Remover Pads
Active ingredientSALICYLIC ACID
Label structure14 sections

Dosage and administration

wash affected area.(optional: may soak wart in warm water for 5 minutes.); dry area thoroughly. (if appropriate: cut plaster to fit wart.); apply medicated plaster; repeat procedure every 48 hours as needed until wart is removed for up to 12 weeks;

Storage and handling

store between 59° and 86°F (15°C and 30°C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Wart and Corn Remover

Use

INDICATIONS & USAGE SECTION

For the removal of warts and corns.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

On irritated, infected, or reddened skin; on genital warts or warts on the face; on moles, birthmarks, or warts with hair growing from them; on mucous membranes.

When Using

OTC - WHEN USING SECTION

Avoid eye or face contact. If the product gets into eyes or faces, thoroughly rinse with water.

Stop Use

OTC - STOP USE SECTION

Discomfort persists

Ask Doctor

OTC - ASK DOCTOR SECTION

Diabetes; Poor blood circulation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash affected area.(optional: may soak wart in warm water for 5 minutes.); dry area thoroughly. (if appropriate: cut plaster to fit wart.); apply medicated plaster; repeat procedure every 48 hours as needed until wart is removed for up to 12 weeks;

Other information

STORAGE AND HANDLING SECTION

store between 59° and 86°F (15°C and 30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

hard paraffin, lanolin, phenol, polyvinyl alkyl, vaseline

Questions

OTC - QUESTIONS SECTION

Call 1-646-798-1280

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN3
240559salicylic acid 0.4 MG/MG Medicated PatchSCD3
240559salicylic acid 40 % Medicated PatchSY3

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
83818-004-01Samsali Wart Corn Remover Pads42 in 1 BOXPATCH423

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83818-004SAMSALI WART CORN REMOVER PADS (WART CORN REMOVER PADS) PATCH [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.]3Current NDC, 1 package rows20240921_186314fe-9438-b1f5-e063-6294a90a9903.zip

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
83818-00483818-004-01

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
Samsali Wart Corn Remover PadsWART CORN REMOVER PADSShenzhen Xinxin Yunhai Technology Co., Ltd.186314fe-9438-b1f5-e063-6294a90a99032024-09-19WarningsExact identifier
ndc (package): 83818-004-01
ndc (product): 83818-004
ndc11 (package): 83818000401
spl id: 22744929-7fe4-3193-e063-6394a90af685
spl set id: 186314fe-9438-b1f5-e063-6294a90a9903

Reported adverse events (FAERS/openFDA)#

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