Quality Choice Medicated Corn Removers

Manufacturer
Chain Drug Marketing Association
Effective date
2026-06-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-06-11 05:11:18

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the removal of corns relieves pain by removing corns

Dosage and administration

wash affected area and dry 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
  • if you have poor blood circulation
  • on irritated skin, on any area that is infected or reddened

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

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 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° and 30°C (59° and 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

RECENT MAJOR CHANGES SECTION

.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QC

QUALITY

CHOICE

Medicated

Corn

Removers

Salicylic Acid 40% / Corn Remover

Effective Corn Removal Treatment

Cushions Against Pressure & Friction

9 Pads

9 Medicated Patches

cartoncarton

DailyMed Product Concepts#

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

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
83324-22983324-229-09, 83324-229-01

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
62026-04-15full-release2026-06-01 01:53:51
52026-01-02monthly-update2026-06-03 17:51:17
32025-11-06monthly-update2026-06-03 17:39:48
22025-05-09full-release2026-06-01 01:00:45

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
Salicylic AcidMEDICATED CORN REMOVERChain Drug Marketing Association3402dfc5-bc36-9c2f-e063-6394a90a31742026-06-09WarningsExact identifier
ndc (package): 83324-229-01
ndc (package): 83324-229-09
ndc (product): 83324-229
ndc11 (package): 83324022901
ndc11 (package): 83324022909
spl id: 53d7a46e-2794-c8ff-e063-6294a90ad81c
spl set id: 3402dfc5-bc36-9c2f-e063-6394a90a3174

Reported adverse events (FAERS/openFDA)#

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