SALICYLIC ACID- wart remover gel gel 
Walgreen Company

----------

Walgreens Wart Remover Gel

Active ingredient

Salicylic acid 17%w/w

Purpose

Wart remover

Uses

Warnings

For external use only.

Flammable

keep away from fire and flame

Do not use

  • on moles, birth marks and warts with hair growing from them
  • on mucous membranes such as nose, anus, genitals and lips
  • on irritated, infected or reddened skin
  • on genital warts and warts on the face
  • if you are diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

When using this product

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

if discomfort persists

see your doctor or podiatrist.

Directions

Other information

store between 59°F to 86°F (15°C to 30°C)

Inactive ingredients

camphor, castor oil, ethyl acetate, hydroxypropyl cellulose, hypophosphorous acid, isopropyl alcohol, nitrocellulose, polysorbate 80, SDA 3C ethyl alcohol

Questions?

call 1-866-964-0939

Principle Display Panel

Walgreens

NEW

MAXIMUM STRENGTH

Wart Remover

Gel

Salicylic Acid

NET WT .25 OZ (7 g)

Walmart Wart Remover Gel

SALICYLIC ACID 
wart remover gel gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0219
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 g  in 7 g
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
ALCOHOL (UNII: 3K9958V90M)  
ETHYL ACETATE (UNII: 76845O8NMZ)  
HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PYROXYLIN (UNII: KYR8BR2X6O)  
CASTOR OIL (UNII: D5340Y2I9G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0219-257 g in 1 TUBE; Type 0: Not a Combination Product08/24/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02808/24/2012
Labeler - Walgreen Company (008965063)

Revised: 2/2024
Document Id: 10f817c2-8e3e-5844-e063-6394a90a8a24
Set id: 9d73b428-b6a0-4b11-88b7-36c012d24e62
Version: 6
Effective Time: 20240209
 
Walgreen Company