Salicylic Acid

Manufacturer
ARMY & AIR FORCE EXCHANGE SERVICE
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:38:07

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.

For external use only.

WARNINGS SECTION

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 1-866-964-0939

​Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Exchange Select

Liquid Wart Remover
Salicylic Acid

  • Removes common and plantar warts safely and effectively
  • Easy-to-use, built-in brush applicator

0.31 FL OZ (9 mL)

Exchange Select_Liquid Wart Remover_53-012ES.jpgExchange Select_Liquid Wart Remover_53-012ES.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55301-133-09Salicylic Acid9 mL in 1 BOTTLE, WITH APPLICATORLIQUID97

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
55301-13355301-133-09

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 · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-12-06full-release2026-06-01 00:40:53

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 AcidWART REMOVER LIQUIDARMY & AIR FORCE EXCHANGE SERVICE50d4bb37-db63-4d92-86a3-b4a43f36f9cd2025-10-07WarningsExact identifier
ndc (package): 55301-133-09
ndc (product): 55301-133
ndc11 (package): 55301013309
spl id: 409765b0-b1a8-f7c1-e063-6394a90a528b
spl set id: 50d4bb37-db63-4d92-86a3-b4a43f36f9cd

Reported adverse events (FAERS/openFDA)#

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