Salicylic Acid

Manufacturer
Hudson Health LLC
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:29:23

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wash affected area and dry thoroughly if necessary, cut medicated patch to fit corn apply adhesive side down of medicated patch onto 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 15 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

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

If discomfort persists see your doctor or podiatrist

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
  • apply adhesive side down of medicated patch onto 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 15 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 1-877-237-0194

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

comfortzone

medicated

corn removers

salicylic acid

  • effective corn removal treatment
  • cushions against pressure & friction

18 pads/ 18 medicated patches

Amazon_Corn Removers_52-003AM.jpgAmazon_Corn Removers_52-003AM.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN8
240559salicylic acid 0.4 MG/MG Medicated PatchSCD8
240559salicylic acid 40 % Medicated PatchSY8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72446-002-182023-01-31C16284748780-1f386c64a-2f54-0266-e053-dadaa90a7c1aComfortzone Medicated Corn Remover

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72446-002-18Salicylic Acid18 in 1 PACKAGEPATCH188

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
72446-00272446-002-18

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

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 REMOVERSHudson Health LLCa3eb0589-738d-4954-85c9-472c7124a0162025-12-30WarningsExact identifier
ndc (package): 72446-002-18
ndc (product): 72446-002
ndc11 (package): 72446000218
spl id: 47333e2c-8a04-dae2-e063-6394a90a8e2a
spl set id: a3eb0589-738d-4954-85c9-472c7124a016

Reported adverse events (FAERS/openFDA)#

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