Salicylic Acid

Manufacturer
Hudson Health LLC
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:38:08

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wash affected area, may soak wart in warm water for 5 minutes dry area thoroughly apply small amount of wart remover with applicator to sufficiently cover each wart let dry and repeat this procedure once or twice daily 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

Use

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.

Flammable

SAFE HANDLING WARNING SECTION

  • keep away from fire or flame
  • cap bottle tightly and store at room temperature away heat

Do not use

OTC - DO NOT USE SECTION

  • if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
  • irritated, infected or reddened skin
  • genital warts and warts on the face
  • moles, birthmarks and warts with hair growing from them
  • mucous membranes

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. If product gets into the eyes, flush with water for 15 minutes
  • avoid inhaling vapors

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 warm water for 5 minutes
  • dry area thoroughly
  • apply small amount of wart remover with applicator to sufficiently cover each wart
  • let dry and repeat this procedure once or twice daily until wart is removed for up to 12 weeks

Other information

OTHER SAFETY INFORMATION

store between 20°C to 30°C (68°F to 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-877-237-0194

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

comfortzone

maximum strength

liquid wart remover

salicylic acid

  • removes common & plantar warts
  • conventient brush applicator
  • safe & effective

NET 0.31 FL OZ (9mL)

Amazon_Liquid Wart Remover_53-160AM.jpgAmazon_Liquid Wart Remover_53-160AM.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72446-006-09Salicylic Acid9 mL in 1 BOTTLE, WITH APPLICATORLIQUID98

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
72446-00672446-006-09

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
72024-10-15full-release2026-06-01 00:25:45

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 REMOVERHudson Health LLC63b62a7a-1082-4323-bf44-810545792de92025-10-07WarningsExact identifier
ndc (package): 72446-006-09
ndc (product): 72446-006
ndc11 (package): 72446000609
spl id: 409719f1-18fb-a025-e063-6394a90ad715
spl set id: 63b62a7a-1082-4323-bf44-810545792de9

Reported adverse events (FAERS/openFDA)#

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