SALICYLIC ACID- liquid wart remover liquid 
Target Corporation

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Target Liquid Wart Remover

Active ingredient

Salicylic acid 17%w/w

Purpose

Wart remover

Uses

Warnings

For external use only.

Flammable

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

Do not use

  • if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

Do not use on

  • 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

  • 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

discomfort persists

Keep out of reach of children.

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

Directions

Other​ information

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

​Inactive ingredients

flexible collodion containing alcohol and ether

Questions?

Call 1-800-910-6874

Principal Display Panel

UP & UP

Compare to Compound W® Wart Remover

maximum strength

Liquid Wart Remover

Salicylic Acid

helps remove common and plantar warts

0.31 FL. OZ (9mL)

BoxLabel

SALICYLIC ACID 
liquid wart remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-443
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2.1 g  in 14.7 mL
Inactive Ingredients
Ingredient NameStrength
PYROXYLIN (UNII: KYR8BR2X6O)  
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
CASTOR OIL (UNII: D5340Y2I9G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-443-2114.7 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/31/200803/15/2015
2NDC:11673-443-099 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/15/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02812/31/2008
Labeler - Target Corporation (006961700)

Revised: 2/2024
Document Id: 10a8ceed-532c-dec3-e063-6294a90af7bb
Set id: ede81b45-aaf6-408b-ac30-50d1d7dbfd87
Version: 8
Effective Time: 20240205
 
Target Corporation