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Salicylic Acid by Geiss Destin & Dunn Inc.

Dosage form: liquid
Ingredients: SALICYLIC ACID 0.17g in 9mL
Labeler: Geiss Destin & Dunn Inc.
NDC Code: 50804-748

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.

Wart Remover Liquid

Active ingredient

Salicylic acid 17%w/w


Wart Remover


for the removal of common and plantar warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. The plantar wart exists only on the bottom of the foot and interrupts footprint pattern.

For external use only.


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

Do not use

if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

irritated, infected or reddened skin

genital warts and warts on the face

moles, birthmarks and warts with hair growing from them

mucous membranes

When using this product

avoid contact with eyes. If product gets into the eyes, flush with water for 15 minutes
avoid inhaling vapors

Stop use and ask 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, may soak wart in warm water for 5 minutes
dry area thoroughly
apply small amount of wart remover with applicator to sufficiently cover each wart
let dry and repeat this procedure once or twice daily until wart is removed for up to 12 weeks

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


Maximum Strength

Liquid Wart Remover

with Salicylic Acid

  • Safely Elminates Common & Plantar Warts
  • Convenient Applicator Brush
  • Safe & Effective

NET WT 0.31 FL OZ (9 mL)

wart remover liquid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-748
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:50804-748-039 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 May 28, 2018

Further information

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