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Salicylic Acid by Geiss, Destin & Dunn, Inc.

Dosage form: liquid
Ingredients: SALICYLIC ACID 0.17g in 9.8mL
Labeler: Geiss, Destin & Dunn, Inc.
NDC Code: 50804-749

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.

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



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

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Corn & Callus Remover

with Salicylic Acid

3 cushions  1/3 FL OZ(9.8 mL)

corn and callus remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-749
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:50804-749-039.8 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B08/10/2015
Labeler - Geiss, Destin & Dunn, Inc. (076059836)

Geiss, Destin & Dunn, Inc.

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Medically reviewed on Aug 10, 2018

Further information

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