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Salicylic Acid by AmerisourceBergen Drug Corporation

Medically reviewed on Dec 21, 2017

Dosage form: patch
Ingredients: SALICYLIC ACID 40mg
Labeler: AmerisourceBergen Drug Corporation
NDC Code: 46122-524

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 Callus Removers

Active ingredient

Salicylic acid 40%


Callus remover

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


​For external use only.

​Do not use
  • if you are a diabetic
  • have poor blood circulation
  • on irritated skin, on 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 thoroughly
  • if necessary, cut medicated patch to fit callus
  • apply adhesive side down of medicated patch onto callus
  • cover medicated patch with pad
  • after 48 hours, remove medicated patch
  • 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 information

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

​Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol


call 1-888-423-0139

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Good Neighbor Pharmacy 
Callus Removers
Salicylic Acid

  • Callus removal treatment
  • Protect against pressure and pain

4 Medicated Patches/6 Pads

medicated callus removers patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-524
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:46122-524-134 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.