SALICYLIC ACID- wart remover liquid liquid 
AmerisourceBergen Drug Corporation

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.

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Wart Remover Liquid

Active ingredient

Salicylic acid 17%w/w

Purpose

Wart Remover

Uses

Warnings

For external use only.

Flammable

  • keep away from fire or flame
  • cap bottle tightly and store at room temerature away from 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
  • on genital warts and warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes
  • on irritated, infected or reddened skin

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.

Directions

Other information

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

Inactive ingredients

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

Principal Display Planel

Good Neighbor Pharmacy

Maximum Strength

Liquid Wart Remover

Salicylic Acid

Removes Common & plantar Warts

Includes:

Safe and Effective

NET WT 1/2 FL. OZ (15mL)

GNP_Liquid Wart Remover_15mL_WRLBXMHRGNP-2.jpg

SALICYLIC ACID 
wart remover liquid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-236
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
PYROXYLIN (UNII: KYR8BR2X6O)  
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
CASTOR OIL (UNII: D5340Y2I9G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24385-236-6315 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/10/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358B01/10/2012
Labeler - AmerisourceBergen Drug Corporation (007914906)

Revised: 12/2017
Document Id: accec0c3-8407-470e-b6a6-8f7bf6d10883
Set id: c0f1d23b-3d6a-43c4-81d5-6585a214222d
Version: 2
Effective Time: 20171219
 
AmerisourceBergen Drug Corporation