Salicylic Acid

Manufacturer
Premier Brands of America Inc.
Effective date
2026-01-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:33:25

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 disc to fit the corn. carefully apply the medicated with sticky side onto the corn cover the medicated disc with the center of the bandage strip. after 48 hours, remove the medicated bandage strip. repeat this 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 re...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40% w/w

Purpose

OTC - PURPOSE SECTION

Corn remover

Use

INDICATIONS & USAGE SECTION

  • for the removal of 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

Stop use and ask a doctor if

OTC - STOP USE 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 area thoroughly.
  • if necessary, cut medicated disc to fit the corn.
  • carefully apply the medicated with sticky side onto the corn
  • cover the medicated disc with the center of the bandage strip.
  • after 48 hours, remove the medicated bandage strip.
  • repeat this 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 59° and 86°F (15° and 30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, polyethylene foam.

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Premier Solutions

Medicated Clear

Corn Removers

SALICYLIC ACID 40%

MAXIMUM

STRENGTH

Effective corn removal treatment

Conceals & protects

Medicated disc, no-mess application

6 MEDICATED DISCS | 6 CLEAR STRIPS

Image 1Image 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN6
240559salicylic acid 0.4 MG/MG Medicated PatchSCD6
240559salicylic acid 40 % Medicated PatchSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56104-258-01Salicylic Acid6 in 1 PACKAGEPATCH66

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
56104-25856104-258-01

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
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-11-03monthly-update2026-06-03 17:39:03
42024-10-14full-release2026-06-01 00:25:27

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 AcidCLEAR MEDICATED CORN REMOVERSPremier Brands of America Inc.f5626988-a23d-44ea-e053-2a95a90a6bd02026-01-15WarningsExact identifier
ndc (package): 56104-258-01
ndc (product): 56104-258
ndc11 (package): 56104025801
spl id: 487529d8-aa2f-4859-e063-6394a90ab30b
spl set id: f5626988-a23d-44ea-e053-2a95a90a6bd0

Reported adverse events (FAERS/openFDA)#

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