TXL Active Wart Remover Pads

Manufacturer
Kairos Trading Inc
Effective date
2023-05-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:55:00

Label at a glance#

ProductTXL Active Wart Remover Pads
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

wash affected area: may soak wart in warm water for 5 minutes dry area thoroughly remove bandage strips by peeling backing off If necessary, cut medicated patch to fit wart carefully apply medicated plaster repeat procedure every 48 hours as needed (until wart is removed) for up to 12 week

Storage and handling

Store between 59° and 86°F (15° and 30°C).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Wart Remover

Use

INDICATIONS & USAGE SECTION

For the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance of the surface.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

When Using

OTC - WHEN USING SECTION

Ask a doctor before use if you have
diabetes poor blood circulatio

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: may soak wart in warm water for 5 minutes
dry area thoroughly
remove bandage strips by peeling backing off
If necessary, cut medicated patch to fit wart
carefully apply medicated plaster
repeat procedure every 48 hours as needed (until wart is removed) for up to 12 week

Other information

STORAGE AND HANDLING SECTION

Store between 59° and 86°F (15° and 30°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

hard paraffin, lanolin, phenol

Questions

OTC - QUESTIONS SECTION

1-914-875-2018

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83124-002-0183124-002-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN1
240559salicylic acid 0.4 MG/MG Medicated PatchSCD1
240559salicylic acid 40 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83124-003-012024-07-30C16284748780-11030e365-42f2-111a-e063-dadaa90a10e283124-003
83124-003-012024-01-30C16284748780-11030e365-42f2-111a-e063-dadaa90a10e283124-003

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83124-003-01TXL Active Wart Remover Pads30 in 1 BOXPATCH301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83124-003TXL ACTIVE WART REMOVER PADS (WART REMOVER PADS) PATCH [KAIROS TRADING INC]11 package rows20230519_fbe70904-6f6d-2c1a-e053-6294a90aeddb.zip

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
83124-00383124-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
PARAFFINI9O0E3H2ZEIACT
LANOLIN7EV65EAW6HIACT
PHENOL339NCG44TVIACT

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
fbe6de4f-a0df-7a51-e053-6394a90a22fcfbe70904-6f6d-2c1a-e053-6294a90aeddb2023-05-17WarningsExact identifier
spl id: fbe6de4f-a0df-7a51-e053-6394a90a22fc
spl set id: fbe70904-6f6d-2c1a-e053-6294a90aeddb

Reported adverse events (FAERS/openFDA)#

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