Quality Choice Medicated Plantar Wart Remover

Manufacturer
Chain Drug Marketing Association
Effective date
2026-06-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-06-11 05:11:19

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.

Dosage and administration

wash affected area, may soak wart in warm water for 5 minutes dry area thoroughly if necessary, cut medicated patches to fit wart apply the adhesive side of patch onto wart cover patch with pads to conceal area repeat 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

Plantar wart remover

​Uses

INDICATIONS & USAGE SECTION

  • for the removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.

​Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • if you are diabetic or have poor blood circulation, except under the advise and supervision of a doctor or podiatrist
  • on irritated, infected or reddened skin

  • on genital warts and warts on the face

  • on moles, birthmarks and warts with hair growing from them

  • on mucous membranes

Keep this and all drugs out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

If discomfort persists 

OTC - ASK DOCTOR SECTION

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 patches to fit wart
  • apply the adhesive side of patch onto wart
  • cover patch with pads to conceal area
  • repeat 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)

​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

QC Quality Choice
Medicated

PLANTAR WART

REMOVER

Salicylic Acid

For Feet:

Cushions, conceals and protects while removing warts

Maxium strength formula without the mess of liquids


24 Medicated Patches

24 Cushioning Pads

Quality Choice_Plantar Wart Remover_PWRBQC.jpgQuality Choice_Plantar Wart Remover_PWRBQC.jpg

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
63868-04263868-042-24

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-12-11full-release2026-06-01 00:42:30

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 AcidMEDICATED PLANTAR WART REMOVERChain Drug Marketing Associationae38c7b0-d5c8-4f1f-ab4d-8e8ea5a095c12026-06-09WarningsExact identifier
ndc (package): 63868-042-24
ndc (product): 63868-042
ndc11 (package): 63868004224
spl id: 53d7f810-f474-2c21-e063-6294a90a63a2
spl set id: ae38c7b0-d5c8-4f1f-ab4d-8e8ea5a095c1

Reported adverse events (FAERS/openFDA)#

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