Wart & Corn Remover

Manufacturer
HONG KONG FOREVER YOUNG TRADING CO., LIMITED
Effective date
2026-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-13 04:03:29

Label at a glance#

ProductWart Corn Remover
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Warnings For external use only. Flammable. Keep away from fire or flame.

Do not use

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

When using this product Avoid contact with eyes. If product gets into eyes, flush with water for 15 minutes.

Stop use and ask a doctor if Discomfort persists.

Ask a doctor before use if you have diabetes or poor blood circulation.

INACTIVE INGREDIENT SECTION

Alcohol
Camphor
Castor Oil
Ethylcellulose
Menthol
Polysorbate 80

INDICATIONS & USAGE SECTION

Uses:
For the removal of corns and calluses.
Relieves pain by removing corns and calluses.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

OTC - PURPOSE SECTION

Purpose: Corn and callus remover (keratolytic)

DOSAGE & ADMINISTRATION SECTION

Directions

Wash affected area. May soak corn or callus in warm water for 5 minutes to assist removal. Dry thoroughly.
Apply one drop at a time to sufficiently cover each corn/callus. Let dry.
Repeat once or twice daily as needed, up to 12 weeks.
May use a pumice stone, file or emery board to gently remove dead softened tissue every few days.

RECENT MAJOR CHANGES SECTION

Directions

Wash affected area. May soak corn or callus in warm water for 5 minutes to assist removal. Dry thoroughly.
Apply one drop at a time to sufficiently cover each corn/callus. Let dry.
Repeat once or twice daily as needed, up to 12 weeks.
May use a pumice stone, file or emery board to gently remove dead softened tissue every few days.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

a aa

Products#

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DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87997-00187997-001-01, 87997-001-02, 87997-001-03, 87997-001-04, 87997-001-05, 87997-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
MENTHOLL7T10EIP3AIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-09-09daily-update2026-09-11 03:01:45

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
5b0cd265-1db7-4d65-e063-6294a90af4255b0cd6e0-f220-4ebd-e063-6294a90ade672026-09-09WarningsExact identifier
spl set id: 5b0cd6e0-f220-4ebd-e063-6294a90ade67

Reported adverse events (FAERS/openFDA)#

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