WART REMOVER

Manufacturer
Shenzhen Hanchuan e-commerce Co., Ltd
Effective date
2025-07-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:07:00

Label at a glance#

ProductWART REMOVER
Active ingredientSALICYLIC ACID
Label structure12 sections

Storage and handling

Out of direct sunlight and storeat room temperature away fromheat.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

WART REMOVER

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1%

OTC - PURPOSE SECTION

Wart Remover

INDICATIONS & USAGE SECTION

For the removal of genital,plantar, common, and flat warts.
The common wart is easilyrecognized by the rough "cauli-flower-like" appearance of thesurface.
The plantar wart is recognizedby its location only on thebottom of the foot, its tender-ness and the interruption of thefootprint pattern.

WARNINGS SECTION

For extemal use only.

Keep away from fire and flame.

OTC - WHEN USING SECTION

Avoid contact with eyes. If theproduct gets into the eye, flushwith water for 15 minutese.
Avoid inhaling vapors.
Cap the tube tightly.
Out of direct sunlight and storeat room temperature away fromheat.

OTC - STOP USE SECTION

lf discomfort persistself you have diabetes or poor blood circulation.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowedget medical help orcontact a Poison Control Center(1-800-222-1222)right away

DOSAGE & ADMINISTRATION SECTION

.Wash the affectod area May soakthe wart in warm water for 5minutes Dry area thoroughly Usingthe applicator (cottonswab), apply alayer of ointment to sufficientlycover each wart ·Allow it to fullyabsorb and cover it with a bandageas needed Repeat this procedureonce or twice daily as needed (untilthe wart is removed) for up to 12weeks

STORAGE AND HANDLING SECTION

Out of direct sunlight and storeat room temperature away fromheat.

INACTIVE INGREDIENT SECTION

Water
Alcohol
Glycerin
Propylene Glycol
Dimethyl Isosorbide
Erythritol
Phenoxyethanol
Aloe Yohjyu Matsu Ekisu
Glyceryl Glucoside
Portulaca Oleracea Extract
Gentiana Scabra Root Extract
Xanthan Gum
Retinoic Acid
Dipotassium Glycyrrhizate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047362salicylic acid 1 % Topical SolutionPSN3
1047362salicylic acid 10 MG/ML Topical SolutionSCD3
1047362salicylic acid 1 % Topical SolutionSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b80ad7bc-1b6f-7ef4-1ed0-86cd9f459d60Product name620251124
1426d8f8-b7d5-4053-8554-613df00c0d86Product name220250616
0e7b8bf1-c46c-4de6-b26a-0c50e34364ecProduct name220250521
e3af9708-3004-7392-4046-5311eaa8bab5Product name320221128
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
503b047e-e62d-4745-9011-522b13bc701bProduct name120181206
7d41caa2-0b5d-9b03-ab8d-84271de26ef4Product name220170314
50ca9ff5-82dd-9971-4f2c-5845a76a8572Product name220150818
0a8118e4-08c6-b395-9ddc-d3e425e0493aProduct name120140508
233bcb0a-cf40-b0a1-b346-c83ac2f43579Product name120140508
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84302-001-01WART REMOVER30 mL in 1 BOTTLELIQUID303

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84302-00184302-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
39a3e2b8-2f7f-e459-e063-6294a90aa5f7180398e3-610a-d796-e063-6394a90a827b2025-07-11WarningsExact identifier
spl id: 39a3e2b8-2f7f-e459-e063-6294a90aa5f7
spl set id: 180398e3-610a-d796-e063-6394a90a827b

Reported adverse events (FAERS/openFDA)#

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