FDA.reportPublic FDA data

Aetna Callus Remover

Manufacturer
Aetna Felt Corp
Effective date
2013-04-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:40:53

Label at a glance#

ProductAetna Callus Remover
Active ingredientSALICYLIC ACID
Label structure6 sections

Indications and uses

For removal of calluses relieves pain by removing calluses

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

Purpose

OTC - PURPOSE SECTION

Callus Removal

Uses

INDICATIONS & USAGE SECTION

  • For removal of calluses
  • relieves pain by removing calluses

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use

  • If you are a diabetic
  • If you hae poor blood circulation
  • On irritated skin or any area that is infected or reddened
OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Discomfort lasts
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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions
  • Wash affected area and dry thoroughly
  • If necessary cut medicated disk to fit callus
  • Apply medicated disk with sitcky side adhering to skin
  • Cover medicated disk with enclosed cushion
  • After 48 hours, remove medicated disk
  • 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Vinyl Acetate

Box Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Good Sense Callus RemoverGood Sense Callus Remover

SPL UNCLASSIFIED SECTION

Hill Country Callus RemoverHill Country Callus Remover

SPL UNCLASSIFIED SECTION

PedX Callus RemoverPedX Callus Remover

SPL UNCLASSIFIED SECTION

Preferred Plus Callus RemoverPreferred Plus Callus Remover

SPL UNCLASSIFIED SECTION

Hill Country Thick Callus RemoverHill Country Thick Callus Remover

SPL UNCLASSIFIED SECTION

PedX Thick Callus RemoverPedX Thick Callus Remover

SPL UNCLASSIFIED SECTION

Smart Sense Thick Callus RemoverSmart Sense Thick Callus Remover

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43345-003-032020-10-07C16284748780-19d75b9d0-e017-f424-e053-dadaa90a57cea465fddf-ed7e-4fc8-a623-9174dceeb879
43345-003-032020-01-31C16284748780-19d75b9d0-e017-f424-e053-dadaa90a57cea465fddf-ed7e-4fc8-a623-9174dceeb879

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ2
VINYL ACETATEINACTIVE INGREDIENTL9MK238N772

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43345-00343345-003-03

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
VINYL ACETATEL9MK238N77IACT

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
b119cbce-d1aa-e7a3-e053-2a95a90a780ea465fddf-ed7e-4fc8-a623-9174dceeb8792020-10-07WarningsExact identifier
spl set id: a465fddf-ed7e-4fc8-a623-9174dceeb879

Reported adverse events (FAERS/openFDA)#

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