KPP ULTRA THICK MEDICATED CALLUS REMOVER- salicylic acid plaster 
Cardinal Health

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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KPP Ultra Thick Medicated Callus Removers

Active Ingredient

Salicylic Acid 40%

Purpose

Callus Removal

Uses

  • For removal of calluses
  • relieves pain by removing calluses

Warnings

For external use only.

Do not use

  • If you are a diabetic
  • If you hae poor blood circulation
  • On irritated skin or any area that is infected or reddened

Stop use and ask a doctor if

  • Discomfort lasts

Keep out of reach of children

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

Directions

  • Wash affected area and dry thoroughly
  • If necessary cut medicated disk to fit callus
  • Apply medicated disk with sitcky side adhering to skin
  • Cover medicated disk with enclosed cushion
  • After 48 hours, remove medicated disk
  • Repeat procedure every 48 hours as needed for up to 14 days(until callus is removed)
  • May soak callus in warm water for 5 minutes to assist in removal

Other

Store between 16° and 30° C (59° and 88° F)

Inactive ingredients

Vinyl Acetate

Preferred Plus Extra Thick Medicated Callus Remover

Box Label

KPP ULTRA THICK MEDICATED CALLUS REMOVER 
salicylic acid plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61715-071
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 
Inactive Ingredients
Ingredient NameStrength
VINYL ACETATE (UNII: L9MK238N77)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61715-071-044 in 1 PACKET; Type 0: Not a Combination Product10/31/199510/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F10/31/199510/12/2020
Labeler - Cardinal Health (012574513)

Revised: 10/2020
Document Id: b17f2eb1-b864-8258-e053-2a95a90a8aa8
Set id: 699db0c0-ce0b-4e7c-88b0-9a9af444a362
Version: 4
Effective Time: 20201012
 
Cardinal Health