SALICYLIC ACID- wart remover liquid

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active ingredient

Salicylic acid

Purpose

Wart Remover

Use

• 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.

Warnings

For external use only.

Flammable

• 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 podiatristirritated, 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.

​Directions

• 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

Questions?

Call 1-866-964-0939

​Principal Display Panel

Premier Value

Maximum Strength

Liquid Wart Remover
with Salicylic acid

60% More than Compound W

Removes common & plantar warts safely

1/2 FL OZ (15mL)

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-611
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.17 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
PYROXYLIN (UNII: KYR8BR2X6O)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CASTOR OIL (UNII: D5340Y2I9G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-611-00	15 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	05/23/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	05/23/2003

Labeler - Chain Drug Consortium, LLC (101668460)