Medicated Callus Removers

Manufacturer
Meijer Distribution Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:29:01

Label at a glance#

ProductMedicated Callus Removers
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of calluses relieves pain by removing calluses

Dosage and administration

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

Callus remover

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

Ask your doctor

OTC - ASK DOCTOR SECTION

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

Other information

OTHER SAFETY INFORMATION

  • store between 15°C to 30°C (59° to 86°F)
  • avoid surrounding skin when applying medicated patch

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

Meijer

Medicated

Maximum Strength

callus remover

SALICYLIC ACID 40%/

Callus Remover

Effective Callus Remover Treatment

Protects Against Pressure & Friction

6 PADS

4 MEDICATED PATCHES

image 1image 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN5
240559salicylic acid 0.4 MG/MG Medicated PatchSCD5
240559salicylic acid 40 % Medicated PatchSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0609-1Medicated Callus Removers1 g in 1 PATCHPATCH15
79481-0609-1Medicated Callus Removers4 in 1 CARTONPATCH45

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-060979481-0609-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-10-30monthly-update2026-06-03 17:39:04
32024-10-14full-release2026-06-01 00:25:01

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
Medicated Callus RemoversSALICYLIC ACIDMeijer Distribution Inc.0399ebde-c7d1-f73d-e063-6294a90a020f2025-12-30WarningsExact identifier
ndc (package): 79481-0609-1
ndc (product): 79481-0609
ndc11 (package): 79481060901
spl id: 4732c7db-b769-b993-e063-6294a90aab3b
spl set id: 0399ebde-c7d1-f73d-e063-6294a90a020f

Reported adverse events (FAERS/openFDA)#

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