Salicylic Acid

Manufacturer
Premier Brands of America Inc.
Effective date
2021-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:08

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wash affected area: may soak corn in warm water for 5 minutes dry area thoroughly remove bandage strips by peeling backing off at slit carefully adhere bandage with the medicated portion directly over corn after 48 hours remove medicated bandage strip repeat this procedure every 48 hours as needed (until corn is removed) for up to 14 days

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
  • have poor blood circulation
  • on irritated skin or any area that is infected or reddened

​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.

OTC - STOP USE SECTION

If discomfort persists see your doctor or podiatrist.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area: may soak corn in warm water for 5 minutes
  • dry area thoroughly
  • remove bandage strips by peeling backing off at slit
  • carefully adhere bandage with the medicated portion directly over corn
  • after 48 hours remove medicated bandage strip
  • repeat this procedure every 48 hours as needed (until corn is removed) for up to 14 days

​Other information

OTHER SAFETY INFORMATION

store between 59° to 86°F (15° to 30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, brown iron oxide, polyethylene foam

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

​Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Premier

Medicated

ONE-STEP CORN

REMOVERS

Salicylic Acid

Effective corn removal treatment

Medicated bandage conceals & protects

One-step, no mess application

Tan Bandage

8 Medicated Bandages


one step corn removerone step corn remover

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN1
240559salicylic acid 0.4 MG/MG Medicated PatchSCD1
240559salicylic acid 40 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56104-047-082021-07-23C16284748780-1c7ccaba7-123c-fd44-e053-dadaa90aa01bPremier Brands One-Step Corn Removers Tan

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56104-047-08Salicylic Acid8 in 1 BOXPATCH81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56104-047SALICYLIC ACID (ONE-STEP CORN REMOVER) PATCH [PREMIER BRANDS OF AMERICA INC.]1Legacy NDC, 1 package rows20210215_ba4e0f15-4a4a-95cd-e053-2995a90a0b70.zip

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
56104-04756104-047-08

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
ba4e1707-b3ec-54d9-e053-2995a90a0e1eba4e0f15-4a4a-95cd-e053-2995a90a0b702021-02-01WarningsExact identifier
spl id: ba4e1707-b3ec-54d9-e053-2995a90a0e1e
spl set id: ba4e0f15-4a4a-95cd-e053-2995a90a0b70

Reported adverse events (FAERS/openFDA)#

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