Salicylic Acid

Manufacturer
United Natural Foods, Inc.
Effective date
2024-12-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:43:42

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

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

Use

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

If discomfort persists

OTC - ASK DOCTOR SECTION

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 area thoroughly
  • if necessary, cut medicated patch to fit corn
  • apply adhesive side down of medicated patch onto corn
  • cover medicated patch with cover
  • 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

1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Equaline

medicated
ultra thin
corn remover

pads

salicylic acid

  • therapeutic corn removal treatment
  • ultra thin cushion helps relieve painful shoe pressure and friction
  • specifically designed for tight shoes

9 Medicated Patches/ 9 Pads

Equaline_Corn Removers Ultra Thin_52-056EQ.jpgEqualine_Corn Removers Ultra Thin_52-056EQ.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN3
240559salicylic acid 0.4 MG/MG Medicated PatchSCD3
240559salicylic acid 40 % Medicated PatchSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-137-09Salicylic Acid9 in 1 CELLO PACKPATCH93
41163-137-09Salicylic Acid1 g in 1 POUCHPATCH13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41163-137SALICYLIC ACID (MEDICATED CORN REMOVERS) PATCH [UNITED NATURAL FOODS, INC.]3Current NDC, 2 package rows20241215_fc74e8cb-a7b1-56b3-e053-6394a90a44ae.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
41163-13741163-137-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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 REMOVERSUnited Natural Foods, Inc.fc74e8cb-a7b1-56b3-e053-6394a90a44ae2024-12-12WarningsExact identifier
ndc (package): 41163-137-09
ndc (product): 41163-137
ndc11 (package): 41163013709
spl id: 2916a19c-d42f-5c70-e063-6394a90a3afa
spl set id: fc74e8cb-a7b1-56b3-e053-6394a90a44ae

Reported adverse events (FAERS/openFDA)#

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