SALICYLIC ACID- wart remover plaster

Salicylic acid by

Drug Labeling and Warnings

Salicylic acid by is a Otc medication manufactured, distributed, or labeled by Topco Associates LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%w/w

Purpose

Wart remover

Use

for the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface.

Warnings

For external use only.

Do not use

• on irritated, infected or reddened skin
• on genital warts and warts on the face
• on moles, birthmarks and warts with hair growing from them
• on mucous membranes such as nose, anus, genitals and lips

​Ask a doctor before use if you have

• diabetes
• poor blood circulation

Stop use and ask a doctor if

discomforts 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
• remove bandage strips by peeling backing off at slit
• adhere medicated patch directly over wart
• repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

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

Inactive ingredients

acrylic adhesive, polyethylene foam

Questions?

call 1-866-964-0939

Principal Display Panel

TopCare

Medicated
Wart Removers

System

Salicylic Acid

• Double disk method removes and conceals warts
• Fast acting formula without the mess of liquids

18 Medicated Patches

20 Concealing Pads

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
wart remover plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 36800-377
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.4 g  in 18

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 36800-377-14	18 in 1 BOX; Type 0: Not a Combination Product	12/06/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	12/06/2017

Labeler - Topco Associates LLC (006935977)