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Salicylic Acid by Kroger Co.

Dosage form: liquid
Ingredients: SALICYLIC ACID 0.17mg in 9mL
Labeler: Kroger Co.
NDC Code: 30142-151

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.

Kroger Corn & Callus Remover Kit

​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, castro oil, ethanol, ethyl ether, nitrocellulose


Call 1-866-964-0939

​Principal Display Panel


Liquid Corn & Callus Remover

Salicylic Acid

  • Removes Corns and Calluses Safely 
  • Cushions Against Pain and Pressure

3 Cushions

0.33 FL OZ (9.8 mL) 

corn and callus remover kit liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-151
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:30142-151-099 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F12/06/2017
Labeler - Kroger Co. (006999528)

Revised: 12/2017
Kroger Co.

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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.