SALICYLIC ACID- liquid wart remover liquid 
Chain Drug Marketing Association Inc.

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Quality Choice 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
  • on genital warts and warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes
  • on irritated, infected or reddened skin

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, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-248-449-9300

Principal Display Panel

QC

Quality Choice

Maximum Strength

Liquid Wart

Remover

Salicylic Acid

Removes Common and Plantar Warts Safely and Easily

Includes Brush Applicator

NET WT 0.31 FL OZ (9 mL)

Liquid Wart RemoverLiquid Wart Remover 2

SALICYLIC ACID 
liquid wart remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-299
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 g  in 9 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:63868-299-099 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02810/01/2015
Labeler - Chain Drug Marketing Association Inc. (011920774)

Revised: 2/2024
Document Id: 106c4dd0-1ac0-9f8e-e063-6294a90a0d67
Set id: 32bfbe17-21e9-4939-b4e0-fdf6acb56ef8
Version: 8
Effective Time: 20240202
 
Chain Drug Marketing Association Inc.