KRONA WART REMOVER

Manufacturer
Consilii LLC
Effective date
2023-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:27:41

Label at a glance#

ProductKRONA WART REMOVER
Active ingredientMETHYL SALICYLATE
Label structure14 sections

Dosage and administration

wash the affected area may soak the wart in warm water for 5 minutes dry area thoroughly using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart allow it to fully absorb and let dry repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Storage and handling

store at room temperature avoid excessive heat 37°C(99°F) skin discoloration any occur during or after use wipe the rim of the bottle with a paper towel between uses

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 7%

Purpose

OTC - PURPOSE SECTION

Wart remover

Use

INDICATIONS & USAGE SECTION

to remove warts such as common warts, plantar warts, fat warts, corns, calluses
the common wart is 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.
Flammable. Keep away from fire and flame.

Do not use

OTC - DO NOT USE SECTION

on irritated skin or on any area that is infected or reddened
on moles, birthmarks, warts with hair growing from them, warts on the face or mucous membranes
if you have diabetes or poor blood circulation

When Using

OTC - WHEN USING SECTION

avoid contact with eyes. If the product gets into the eye, flush with water for 15 minutes
avoid inhaling vapors
cap the bottle tightly and store at room temperature away from heat
out of direct sunlight

Stop Use

OTC - STOP USE SECTION

if discomfort persists.

Ask Doctor

OTC - ASK DOCTOR SECTION

if discomfort persists.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash the affected area
may soak the wart in warm water for 5 minutes
dry area thoroughly
using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart
allow it to fully absorb and let dry
repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Other information

STORAGE AND HANDLING SECTION

store at room temperature
avoid excessive heat 37°C(99°F)
skin discoloration any occur during or after use
wipe the rim of the bottle with a paper towel between uses

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ageratina herbacea, Hawthorn leaf with flower, Lonicera confusa flower, Podophyllum hexandrum root, Pseudolarix amabilis bark, Sophora pachycarpa, Thyme

Questions

OTC - QUESTIONS SECTION

kronasmile@gmail.com

kronabeauty.com

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83299-011-012024-01-30C16284748780-11030e365-597e-111a-e063-dadaa90a10e2020fddaa-bf87-34b3-e063-6294a90a8fab

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83299-01183299-011-01

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
20d17107-8877-e53c-e063-6294a90a58a7020fddaa-bf87-34b3-e063-6294a90a8fab2024-08-29WarningsExact identifier
spl set id: 020fddaa-bf87-34b3-e063-6294a90a8fab

Reported adverse events (FAERS/openFDA)#

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