SALICYLIC ACID- one step clear wart remover plaster 
Chain Drug Consortium, LLC

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Premier Value One Step Wart Removers Clear

Active ingredient

Salicylic acid 40%w/w

Purpose

Wart remover

Use

  • for the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface.

Warnings

For external use only.

Do not use

  • on irritated, infected or reddened skin
  • on genital warts and warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes such as nose, anus, genitals and lips

​Ask a doctor before use if you have

  • diabetes
  • poor blood circulation

​Stop use and ask a doctor if

discomforts persists

​Keep out of reach of children.

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

Directions

  • wash affected area: may soak wart in warm water for 5 minutes
  • dry area thoroughly
  • remove bandage strips by peeling backing off
  • adhere medicated patch directly over wart
  • repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

store between 59°F to 86°F (15°C to 30°C)

Inactive ingredients

acrylic adhesive, polyethylene foam

Questions?

call 1-866-964-0939

Principal Display Panel

Premier Value

Maximum Strength

One Step Wart Remover

Salicylic Acid 40%

CLEAR STRIPS

Safely removes common and plantar warts

Fast acting formula without the mess of liquids

Seals and protects

14 MEDICATED STRIPS

ONE STEP CLEAR WART REMOVER

SALICYLIC ACID 
one step clear wart remover plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-374
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g  in 14 
Inactive Ingredients
Ingredient NameStrength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-374-1414 in 1 BOX; Type 0: Not a Combination Product05/23/200301/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02805/23/200301/31/2023
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 11/2023
 
Chain Drug Consortium, LLC