Medicated Corn Removers

Medicated Corn Removers

Drug Labeling and Warnings

Drug Details

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SALICYLIC ACID- medicated corn removers patch 
Topco Associates 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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Medicated Corn Removers

Active ingredient

Salicylic acid 40%

​Purpose

Corn Remover

​Uses

  • for the removal of corns
  • relieves pain by removing corns

​Warnings

​For external use only.

​Do not use

  • if you are diabetic
  • have poor blood circulation
  • on irritated skin, or any area that is infected or reddened

Stop Use and ​Ask a doctor 

if discomfort persists

Keep out of reach of children.

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

Directions

  • wash affected area and dry area thoroughly
  • if necessary, cut medicated patch to fit corn
  • apply adhesive side down of medicated patch onto corn
  • cover medicated patch with pad
  • after 48 hours, remove medicated patch
  • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
  • may soak corn in warm water for 5 minutes to assist in removal

Other information

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

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

​Questions?

call 1-866-964-0939

​Principal Display Panel

TopCare
Medicated Corn Removers
Salicylic acid

  • Therapeautic corn removal treatment
  • Protects against pressure & pain

9 Medicated Patches/9Pads

Top Care_Corn Removers_52-003TC.jpg

Top Care_Corn Removers_52-003TC.jpg

SALICYLIC ACID 
medicated corn removers patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 36800-021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 9 
Inactive Ingredients
Ingredient NameStrength
POLYVINYL ALCOHOL (UNII: 532B59J990)  
VINYL ACETATE (UNII: L9MK238N77)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 36800-021-099 in 1 PACKAGE; Type 0: Not a Combination Product01/03/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F01/03/2012
Labeler - Topco Associates LLC (006935977)

Revised: 12/2017
 
Topco Associates LLC


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