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Salicylic Acid by Chain Drug Marketing Association Inc.

Dosage form: liquid
Ingredients: SALICYLIC ACID 0.17g in 9.8mL
Labeler: Chain Drug Marketing Association Inc.
NDC Code: 63868-298

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.

Quality Choice Liquid Corn and Callus Remover

​Active ingredient

Salicylic acid 17%w/w


Corn and callus remover

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


​For external use only.

  • keep away from fire or flame
  • cap bottle tightly and store at room temperature away heat

Do not use
  • on irritated skin
  • on any area that is infected or reddened
  • if you are a diabetic, or if you have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

When using this product
  • avoid contact with eyes
  • avoid inhaling vapors
  • if product gets into the eyes, flush with water for 15 minutes

Stop and ask a doctor

if discomfort persists, see your doctor or podiatrist

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
  • apply one drop at a time with applicator, to sufficiently cover each corn/callus; let dry
  • use cushions with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
  • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

​Other information

store between 20°C to 30°C (68°F to 86°F)

​Inactive ingredients

camphor, castor oil, ethanol, ethyl ether, nitrocellulose


Call 1-248-449-9300

Principal Display Panel


Quality Choice

Liquid Corn and Callus Remover

Salicylic Acid

Cushions Against Pain and Pressure

Removes Corns and Calluses Safely

3 Cushions

1/3 FL OZ (9.8 mL)

liquid corn and callus remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-298
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:63868-298-039.8 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B10/01/2015
Labeler - Chain Drug Marketing Association Inc. (011920774)

Revised: 12/2017
Chain Drug Marketing Association Inc.

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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.