Skip to Content

KPP Ultra Thick Medicated Callus Remover

Medically reviewed on June 26, 2018

Dosage form: plaster
Ingredients: SALICYLIC ACID 401
Labeler: Cardinal Health
NDC Code: 61715-071

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.

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

KPP ULTRA THICK MEDICATED CALLUS REMOVER 
salicylic acid plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61715-071(NDC:43345-003)
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID40 
Inactive Ingredients
Ingredient NameStrength
VINYL ACETATE 
Packaging
#Item CodePackage Description
1NDC:61715-071-044 PLASTER in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F10/31/1995
Labeler - Cardinal Health (012574513)

 
Cardinal Health

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide