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Salicylic Acid by AmerisourceBergen Drug Corporation

Medically reviewed by Last updated on Dec 21, 2017.

Dosage form: patch
Ingredients: SALICYLIC ACID 40mg
Labeler: AmerisourceBergen Drug Corporation
NDC Code: 46122-526

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.

Medicated Corn Removers

Active ingredient

Salicylic acid 40%


Corn Remover

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


​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.

  • 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


call 1-866-964-0939

​Principal Display Panel

Good Neighbor Pharmacy
Medicated Corn Removers
Salicylic acid

  • Therapeautic corn removal treatment
  • Protects against pressure & pain

9 Medicated Patches/9Pads

medicated corn removers patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-526
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:46122-526-239 PATCH in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F12/21/2017
Labeler - AmerisourceBergen Drug Corporation (007914906)

AmerisourceBergen Drug Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.