CVS Wart Remover

Manufacturer
CVS Pharmacy
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:55:43

Label at a glance#

ProductWart Remover
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 carefully adhere medicated patch directly over 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 40% w/w

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, infected or reddened skin
  • on genital warts or warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes
  • if you are a diabetic or if you have poor blood circulation

Stop use and ask a doctor if

OTC - ASK DOCTOR 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
  • may soak wart in warm water for 5 minutes
  • dry area thoroughly
  • if necessary, cut medicated patch to fit wart
  • carefully adhere medicated patch directly over 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° and 86°F (15° and 30°C)
  • avoid surrounding skin when applying medicated product

​Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS

Maximum Strength

WART REMOVER
PATCHES

Salicylic Acid 40%

Compare to Dr. Scholl's active ingredient

1) Medicated Patch
Removes Wart

2) Pad Covers & Cushions

Safe & Effective,
No-Mess Treatment

18 MEDICATED PATCHES
20 CONCEALING PADS

cartoncarton

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
51316-757-18Wart Remover18 in 1 BOXPATCH183
51316-757-18Wart Remover1 g in 1 PATCHPATCH13

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
51316-75751316-757-18

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
22026-04-10monthly-update2026-06-03 18:00:31
12026-03-24monthly-update2026-06-03 17:58:57

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
Wart RemoverSALICYLIC ACIDCVS Pharmacy4dcccf04-5c4f-1202-e063-6394a90ab9d82026-04-30WarningsExact identifier
ndc (package): 51316-757-18
ndc (product): 51316-757
ndc11 (package): 51316075718
spl id: 5038a664-53b9-0bc3-e063-6294a90a4e46
spl set id: 4dcccf04-5c4f-1202-e063-6394a90ab9d8

Reported adverse events (FAERS/openFDA)#

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