CLEAR GEL CORN REMOVER- salicylic acid patch 
Chain Drug Consortium, LLC

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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Premier Value Clear Gel Wart Removers

Active Ingredient

Salicylic acid 40%

Purpose

Wart Remvoer

Uses

Warnings

For external use only.

Do not use

  • if you are diabetic
  • have poor blood circulation
  • on irritated skin, on any area that is infected or reddened
  • on genital warts and warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes

Stop use and ask doctor

if discomfort persist

Keep out of reach of children.

If, swallowed , get medical help or cotnact a poison Control Center right away.

Directions

Other Information

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

Inactive Ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions

Call 1-866-964-0939

Principal Display Panel

Premier Value

Medicated

Clear Gel Wart Removers

SALICYLIC ACID 40%

Maximum strength

9 CUSHIONS

12 MEDICATED DISCS

image 1

CLEAR GEL CORN REMOVER 
salicylic acid patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-444
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 6 
Inactive Ingredients
Ingredient NameStrength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
VINYL ACETATE (UNII: L9MK238N77)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-444-126 in 1 PACKAGE; Type 0: Not a Combination Product01/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F01/01/2018
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 1/2023
Document Id: f2a132af-d760-2ca0-e053-2a95a90a332e
Set id: f2a145fd-3e0f-5acf-e053-2995a90af572
Version: 1
Effective Time: 20230119
 
Chain Drug Consortium, LLC