WART REMOVER

Manufacturer
Consilii LLC
Effective date
2023-06-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:30:08

Label at a glance#

ProductWART REMOVER
Active ingredientMETHYL SALICYLATE
Label structure11 sections

Dosage and administration

wash the affected area mey soak the wart in warm water tor 5 minutes Gry area thoroughly using the applicator(cotton swab), apply a layer at Gintment to sufficiently cover each wart allow it to fully absorb and cover it with a bandage as needed. repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

salicylic acid 12%

Purpose

OTC - PURPOSE SECTION

Wart remover

Use

INDICATIONS & USAGE SECTION

for the removal ot common and plantar warts
the common wart ls easily recognized by the rough
cauliflower-like appearance of the surface
the plantar wart is recognized by its location only on
the bottom of the foot, its tenderness and the
interruption of the footprint pattern

Warnings

WARNINGS SECTION

For external use only
Keep away from fire and flame

When Using

OTC - WHEN USING SECTION

avoid contact with eyes. If the product gets into the
eye lush with water for 15 minutes
avoid inhaling vapers
cap the bottle tightly

Stop Use

OTC - STOP USE SECTION

If discomfort persists

Ask Doctor

OTC - ASK DOCTOR SECTION

If you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Oot Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

wash the affected area
mey soak the wart in warm water tor 5 minutes
Gry area thoroughly
using the applicator(cotton swab), apply a layer at
Gintment to sufficiently cover each wart
allow it to fully absorb and cover it with a bandage as
needed.
repeat this procedure once or twice daily as needed
(until the wart is removed) for up to 12 weeks

Inactive ingredients

INACTIVE INGREDIENT SECTION

Watery, Sodiurn bicarbonate
Propylene glycol, Ethanol, Frutus cnidil,
Kuhrseng, Pursiane, The rhizome of
large-headed atractylodes, Radix angelicae,
Pericarpiur citri reticulatae, Asarum,
Fructus forsythiae, Bamboo leat, Platycodon
grandiflorur, xanthan gum

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83299-007-012024-01-30C16284748780-11030e364-fbb1-111a-e063-dadaa90a10e2fe0611db-7adf-9678-e053-6294a90a1153

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83299-00783299-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
20d164b6-ab93-4297-e063-6394a90a0df7fe0611db-7adf-9678-e053-6294a90a11532024-08-29WarningsExact identifier
spl set id: fe0611db-7adf-9678-e053-6294a90a1153

Reported adverse events (FAERS/openFDA)#

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