SALICYLIC ACID WART REMOVER

Manufacturer
CVS Pharmacy
Effective date
2026-01-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:34:59

Label at a glance#

ProductSALICYLIC ACID WART REMOVER
Active ingredientSALICYLIC ACID
Label structure8 sections

Dosage and administration

wash affected area may soak wart in warm water for 5 minutes dry area thoroughly remove medicated pad from backing paper by pulling from center of pad apply repeat procedure every 48 hours as needed until wart is removed for up to 12 weeks. If the wart is still present after 12 weeks consult a physician.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

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 of the surface

Warnings

WARNINGS SECTION

For External Use Only

Do not use

OTC - DO NOT USE SECTION

  • on irritated skin
  • on any area that is infected or reddened
  • on moles
  • on birthmarks
  • on warts with hair growing from them
  • on genital warts
  • on warts on the face
  • on warts on mucous membranes such as inside the mouth, nose, anus, genitals, lips

Ask a doctor before use if you have

OTC - STOP USE SECTION

  • diabetes
  • poor blood circulation

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area
  • may soak wart in warm water for 5 minutes
  • dry area thoroughly
  • remove medicated pad from backing paper by pulling from center of pad
  • apply
  • repeat procedure every 48 hours as needed until wart is removed for up to 12 weeks. If the wart is still present after 12 weeks consult a physician.

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature
  • avoid excessive heat (37ºC, 99ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

lanolin, polybutene, rosin ester, rubber

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS ™

Maximum Strength+

Wart Remover Strips

Salicylic Acid 40%

Compare to Compound W active ingredient

3-in-1 Treatment+Cushion+Waterproof Protection

Efectively Removes Warts

14 MEDICATED PADS

+under OTC monograph

LabelLabel

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
69842-596-01SALICYLIC ACID WART REMOVER14 in 1 POUCHSTRIP146
69842-596-01SALICYLIC ACID WART REMOVER1 in 1 BOXSTRIP16

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
69842-59669842-596-01
51511-596

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SALICYLIC ACID WART REMOVERSALICYLIC ACIDCVS Pharmacy58a95702-364a-4c19-afd8-51973b79ea852026-01-27WarningsExact identifier
ndc (package): 69842-596-01
ndc (product): 69842-596
ndc11 (package): 69842059601
spl id: 49613711-cad9-3b6a-e063-6394a90a7345
spl set id: 58a95702-364a-4c19-afd8-51973b79ea85
Salicylic Acid Wart RemoverSALICYLIC ACIDASO Pharmaceutical Co. Ltd.6f2bbdee-4c68-4138-b52f-c0e4534e79852025-10-17WarningsExact identifier
ndc (product): 51511-596

Reported adverse events (FAERS/openFDA)#

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