Wart Remover

Manufacturer
Ehy Holdings LLC
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:51:12

Label at a glance#

ProductWart Remover
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

Directions : Wash the affected area and dry it Apply this product with a cotton swab to the wart Repeat this procedure twice daily as needed ( until wart is removed ) for up to 12 weeks

Storage and handling

Other information Store at room temperature and out of direct sunlight skin discoloration may occur during or affter use

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 12%

Purpose

OTC - PURPOSE SECTION

Wart remover

Use

INDICATIONS & USAGE SECTION

use :
for the removal of common and plantar warts
the common war is easy ily recognized by the rough macauli flowerlike " appearance of the surface
the plantar wart is recognized by its location only on the bottom ofthe foot . its tenderness and the interru option of the foot pró nt pattern

Warnings

WARNINGS SECTION

Warnings
For externall use

Do not use

OTC - DO NOT USE SECTION

Do not use
on irritated skin or on any area that is infected or reddened
Do not use on moles skin tags , birthmarks , warts with hair growing from them , genital warts , or warts on the face or mucous membranes

OTC - WHEN USING SECTION

Ask a doctor before you use
if you have diabetes or poor blood circulation
Stop use and ask a doctor
if discomfort persists
Keep out of reach of children
If product gets into eyes , flush with water for 15 minutes
IF swallowed , get medical help or contact a Poison Control Center right away

OTC - STOP USE SECTION

Stop use and ask a doctor
if discomfort persists

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children
If product gets into eyes , flush with water for 15 minutes
IF swallowed , get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Directions :
Wash the affected area and dry it
Apply this product with a cotton swab to the wart
Repeat this procedure twice daily as needed ( until wart is removed ) for up to 12 weeks

Other information

STORAGE AND HANDLING SECTION

Other information
Store at room temperature and out of direct sunlight
skin discoloration may occur during or affter use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

BRUCEA JAVANICA FRUIT

Coptis Chinensis Root Extract

Phellodendron Amurense Bark Extract

LONICERA JAPONICA TOP

Triclosan

Borneol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81799-004-01

81799-004-0181799-004-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199213salicylic acid 12 % Topical SolutionPSN1
199213salicylic acid 120 MG/ML Topical SolutionSCD1
199213salicylic acid 12 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81799-004-012024-01-30C16284748780-11030e365-37f9-111a-e063-dadaa90a10e281799-004 Wart Remover

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81799-004-01Wart Remover15 mL in 1 BOTTLELIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81799-004WART REMOVER (ZITALON WART REMOVAL TREATMENT LIQUID) LIQUID [EHY HOLDINGS LLC]1Legacy NDC, 1 package rows20221027_ebda9663-5e58-05f2-e053-2995a90a6f96.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81799-00481799-004-01

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
ebda964a-6984-9082-e053-2a95a90a0e5eebda9663-5e58-05f2-e053-2995a90a6f962022-10-25WarningsExact identifier
spl id: ebda964a-6984-9082-e053-2a95a90a0e5e
spl set id: ebda9663-5e58-05f2-e053-2995a90a6f96

Reported adverse events (FAERS/openFDA)#

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