Salicylic Acid

Manufacturer
Walgreen Company
Effective date
2026-01-20
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:33:55

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wash affected area, may soak wart in warm water for 5 minutes dry area thoroughly if necessary, cut medicated patch to fit wart apply adhesive side down of patch onto wart cover patch with pad to conceal area repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid

Purpose

OTC - PURPOSE SECTION

Wart remover

Use

INDICATIONS & USAGE SECTION

for the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance.

Warnings

WARNINGS SECTION

For external use only.

Do not use this product if

OTC - DO NOT USE SECTION

  • you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

Do not use on

OTC - DO NOT USE SECTION

  • irritated, infected or reddened skin
  • moles, birthmarks and warts with hair growing from them
  • genital warts and warts on face
  • mucous membranes

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.

Stop and ask a doctor

OTC - ASK DOCTOR SECTION

If discomfort persists see your doctor or podiatrist

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area, may soak wart in warm water for 5 minutes
  • dry area thoroughly
  • if necessary, cut medicated patch to fit wart
  • apply adhesive side down of patch onto wart
  • cover patch with pad to conceal area
  • repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

rubber-based adhesive

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Well at Walgreens

MEDICATED

Wart Remover

Salicylic Acid 40%

  • Patch & pad treatment removes warts
  • No mess of liquids
  • Safe & effective

18 MEDICATED PATCHES | 20 CONCEALING PADS

WAL_Wart Removers_WRBW-3.jpgWAL_Wart Removers_WRBW-3.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN9
240559salicylic acid 0.4 MG/MG Medicated PatchSCD9
240559salicylic acid 40 % Medicated PatchSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0203-18Salicylic Acid18 in 1 BOXPATCH189

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
0363-02030363-0203-18

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-11-06monthly-update2026-06-03 17:38:52
72024-12-13full-release2026-06-01 00:43:14

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 AcidWART REMOVERSWalgreen Company5ef4636b-9ff1-4ac5-818d-4fd547de7de62026-01-20WarningsExact identifier
ndc (package): 0363-0203-18
ndc (product): 0363-0203
ndc11 (package): 00363020318
spl id: 48d42590-0ceb-d5fe-e063-6294a90a72af
spl set id: 5ef4636b-9ff1-4ac5-818d-4fd547de7de6

Reported adverse events (FAERS/openFDA)#

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