SALICYLIC ACID- salicylic acid liquid 
Target Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

Liquid Wart Remover

salicylic acid

Compare to Compound W® Wart Remover

maximum strength
helps remove common and plantar warts
convenient applicator
painless, safe and effective

liquid wart remover
salicylic acid
.5 FL OZ (14.7mL)

up & up Liquid Wart Remover label.jpg

up & up Liquid Wart Remover box.jpg

SALICYLIC ACID 
liquid wart remover liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:11673-443
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID2.1 g  in 14.7 mL
Inactive Ingredients
Ingredient NameStrength
PYROXYLIN 
CAMPHOR (NATURAL) 
CASTOR OIL 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-443-2114.7 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B12/31/2008
Labeler - Target Corporation (006961700)

Revised: 9/2013
Document Id: 1f5c7e39-b321-4e74-a395-e43c2587debb
Set id: ede81b45-aaf6-408b-ac30-50d1d7dbfd87
Version: 2
Effective Time: 20130911
 
Target Corporation