SALICYLIC ACID- wart remover liquid 
Chain Drug Consortium, LLC

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Premier Value Liquid Wart Remover

​Active ingredient

Salicylic acid

Purpose

Wart Remover

Use

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 podiatristirritated, 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

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

​Principal Display Panel

Premier Value

Maximum Strength

Liquid Wart Remover
with Salicylic acid

60% More than Compound W

Removes common & plantar warts safely

1/2 FL OZ (15mL)

PV Liq Wart REMOVER box.jpgPV LIq Wart REMOVER label.jpg

SALICYLIC ACID 
wart remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-611
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 mg  in 15 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:68016-611-0015 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product05/23/2003
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02805/23/2003
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2024
Document Id: 106a7de4-8bde-7906-e063-6294a90ae239
Set id: 3b489e3e-f013-414a-96fe-7936008850a9
Version: 11
Effective Time: 20240202
 
Chain Drug Consortium, LLC