Wart Remover-SALICYLIC ACID

Manufacturer
Ecommerce Digital Sales LLC
Effective date
2026-02-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:47:21

Label at a glance#

ProductWart Remover-SALICYLIC ACID
Active ingredientSALICYLIC ACID
Label structure14 sections

Indications and uses

For the removal of common warts and plantar warts. The common wart is easily recognized by the rough ''cauliflower-like'' appearance of surface The planter wart is recognized by its location only on the bottom of foot, its tenderness, & interruption of footprint pattern

Dosage and administration

Wash affected area (may soak wart in warm water for 5 minutes) Dry area thoroughly Using the applicator, apply a small amount of the product to sufficiently cover each wart & let it dry Use once or twice daily as needed until wart is removed  Wart removal may take upto 12 weeks  Children under 2 years: ask a doctor 

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid.......17%

PURPOSE:

OTC - PURPOSE SECTION

Wart Remover 

USES:

INDICATIONS & USAGE SECTION

For the removal of common warts and plantar warts.

  • The common wart is easily recognized by the rough ''cauliflower-like'' appearance of surface
  • The planter wart is recognized by its location only on the bottom of foot, its tenderness, & interruption of footprint pattern

WARNING:

WARNINGS SECTION

For external use only.

DO NOT USE: 

OTC - DO NOT USE SECTION

  • On irritated skin or any area that is infected 
  • If you are diabetic or have poor blood circulation
  • On birthmarks, moles, warts with hair growing from them, genital warts, warts on face, or warts on mucus membranes

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

  • Avoid contact with eyes and mucus membrans 
  • if burning,discomfort or irritation occurs, stop use & ask a doctor 
  • Cap bottle tightly after use
  • Flammble-keep away from heat and flame

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

  • Discomfort persists
  • Excessive irritation occurs 
  • You do not see improvement within 12 weeks 

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

DIRECTIONS 

DOSAGE & ADMINISTRATION SECTION

  • Wash affected area (may soak wart in warm water for 5 minutes)
  • Dry area thoroughly
  • Using the applicator, apply a small amount of the product to sufficiently cover each wart & let it dry
  • Use once or twice daily as needed until wart is removed 
  • Wart removal may take upto 12 weeks 
  • Children under 2 years: ask a doctor 

OTHER INFORMATION:

OTHER SAFETY INFORMATION

  • Store at 20-25 °C (68-77 °F)
  • Keep cap tightly closed;avoid contact with fabrics surfaces 
  • Protect from freezing and excessive heat
  • Tamper evident: do not use if seal is broken or missing

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water, Gycerin, Polyethylene Glycol, Borneol

QUESTIONS ?

OTC - QUESTIONS SECTION

1-800-534-1894

NDC 87295-0001-1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

skin tag remover 1 Pack outlinedskin tag remover 1 Pack outlined

NDC 87295-0001-2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

skin tag remover 2 Pack outlinedskin tag remover 2 Pack outlined

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN2
312881salicylic acid 170 MG/ML Topical SolutionSCD2
312881salicylic acid 17 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87295-0001-1Wart Remover-SALICYLIC ACID30 mL in 1 BOTTLE, WITH APPLICATORLIQUID302
87295-0001-1Wart Remover-SALICYLIC ACID1 in 1 CARTONLIQUID12
87295-0001-2Wart Remover-SALICYLIC ACID30 mL in 1 BOTTLE, WITH APPLICATORLIQUID302
87295-0001-2Wart Remover-SALICYLIC ACID2 in 1 CARTONLIQUID22

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87295-000187295-0001-1, 87295-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
51972e61-bdfd-467c-a23e-dd6aeefb815cf51666ff-5ee5-4dc9-9b05-b52f54be8a212026-07-07WarningsExact identifier
spl set id: f51666ff-5ee5-4dc9-9b05-b52f54be8a21

Reported adverse events (FAERS/openFDA)#

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