FDA.reportPublic FDA data

Target Liquid Wart Remover

Manufacturer
Target Corporation
Effective date
2026-06-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-07-17 21:36:59

Label at a glance#

ProductSalicylic acid
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the removal of common warts and plantar warts on the bottom of the foot. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. 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 wam water for 5 minutes dry area thoroughly carefully apply one drop at a time with applicator to sufficiently cover each wart let dry repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%w/w

Purpose

OTC - PURPOSE SECTION

Wart remover

Uses

INDICATIONS & USAGE SECTION

  • for the removal of common warts and plantar warts on the bottom of the foot. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. 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.

Flammable

SAFE HANDLING WARNING SECTION

  • keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

  • if you are a diabetic or if you have poor blood circulation
  • on genital warts or warts on the face or mucous membrane
  • on moles, birthmarks or warts with hair growing from them
  • on irritated skin or on any area that is infecred or reddened
​When using this product

OTC - WHEN USING SECTION

  • If product gets into the eyes, flush with water for 15 minutes
  • avoid inhaling vapors
  • cap bottle tightly and store at room temperature away from heat
​Stop use and ask doctor if

OTC - STOP USE 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 wam water for 5 minutes
  • dry area thoroughly
  • carefully apply one drop at a time with applicator to sufficiently cover each wart
  • let dry
  • repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Other​ information

OTHER SAFETY INFORMATION

  • store between 20° - 25°C (68°- 77°F)
  • close tightly to prevent solidification
  • wipe top of bottle clean after each use
  • discard when signs of wart no longer appear
  • avoid surrounding skin when applying product
  • do not allow to come into contact with fabrics, floors, countertops or other surfaces--will stain

​Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

..

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredient

in Compound W®*

Maximum Strength

Liquid Wart

Remover

Salicylic Acid 17% / Wart Remover

  • Removes common and plantar warts
  • Safe and effective

NET 0.31 FL. OZ. (9 mL)

cartoncarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130492450604912GTIN-13: 0492450604912
EAN-13: 0492450604912
GTIN-12: 492450604912
UPC-A: 492450604912
GTIN storage (14 digits): 00492450604912		Target_upupLiquid Wart Remover.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-40382442-403-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ETHYL ETHER0F5N573A2YIACT
SALICYLIC ACIDO414PZ4LPZACTIB
NITROCELLULOSEKYR8BR2X6OIACT
CAMPHOR (NATURAL)N20HL7Q941IACT
CASTOR OILD5340Y2I9GIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-10-07full-release2026-06-01 01:38:05
12025-06-10full-release2026-06-01 01:03:07

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 acidLIQUID WART REMOVERTarget Corporation3779459d-b8e5-6c96-e063-6294a90a116c2026-06-29WarningsExact identifier
ndc (package): 82442-403-01
ndc (product): 82442-403
ndc11 (package): 82442040301
spl id: 54dcd739-21dc-9d5f-e063-6294a90a20a4
spl set id: 3779459d-b8e5-6c96-e063-6294a90a116c

Reported adverse events (FAERS/openFDA)#

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