FDA.reportPublic FDA data

Medicated Corn Removers

Manufacturer
Premier Brands of America, Inc.
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:52:38

Label at a glance#

ProductMedicated Corn Removers
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of corns relieves pain by removing corns

Dosage and administration

wash affected area and dry area thoroughly if necessary, cut medicated patch to fit corn carefully adhere medicated patch directly over corn cover medicated patch with pad after 48 hours, remove medicated patch repeat procedure every 48 hours as needed for up to 14 days (until corn is removed) may soak corn in warm water for 5 minutes to assist in removal

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Corn remover

Uses

INDICATIONS & USAGE SECTION

  • for the removal of corns
  • relieves pain by removing corns

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • if you are diabetic
  • have poor blood circulation
  • on irritated skin, or any area that is infected or reddened

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if discomfort persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area and dry area thoroughly
  • if necessary, cut medicated patch to fit corn
  • carefully adhere medicated patch directly over corn
  • cover medicated patch with pad
  • after 48 hours, remove medicated patch
  • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
  • may soak corn in warm water for 5 minutes to assist in removal

Other information

OTHER SAFETY INFORMATION

store between 15°C to 30°C (59°F to 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

medicated

corn removers

salicylic acid 40%

cushioned pads help protect against pressure and friction

effective corn removal treatment

9 MEDICATED PATCHES / 9 PADS

image 1image 1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56104-249MEDICATED CORN REMOVERS (SALICYLIC ACID) PATCH [PREMIER BRANDS OF AMERICA, INC.]4Legacy NDC20241016_e3b198f5-c3eb-9836-e053-2995a90afaf5.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56104-24956104-249-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYVINYL ALCOHOL532B59J990IACT
VINYL ACETATEL9MK238N77IACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
3bba6d23-9d9f-6f4a-e063-6394a90aa24ce3b198f5-c3eb-9836-e053-2995a90afaf52025-08-06WarningsExact identifier
spl set id: e3b198f5-c3eb-9836-e053-2995a90afaf5

Reported adverse events (FAERS/openFDA)#

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