SALICYLIC ACID- wart remover plaster

Salicylic acid by

Drug Labeling and Warnings

Salicylic acid by is a Otc medication manufactured, distributed, or labeled by HY-VEE, INC. 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

HyVee

health

Wart Remover

Salicylic Acid

Medicated

• Patch/Pad Method Covers & Removes Warts
• No Mess of Liquids
• Safe & Effective

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: 42507-133
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: 42507-133-14	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 - HY-VEE, INC (006925671)