MAXIMUM STRENGTH WART REMOVER STRIPS- one step wart remover plaster

Maximum Strength Wart Remover Strips by

Drug Labeling and Warnings

Maximum Strength Wart Remover Strips by is a Otc medication manufactured, distributed, or labeled by Hudson Health 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 and plantar warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface.

Warnings

For external use only.

Do not use

• if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

Keep out of reach of children

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

Stop use and ask a doctor

If discomforts persists see your doctor or podiatrist.

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 1-877-237-0194

Principal Display Panel

comfortzone

maximum strength

one-step wart remover

salicylic acid

• effective wart removal treatment
• medicated strips cover & remove warts
• one-step application without the mess of liquids
• seals & protects

14 medicated strips

INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH WART REMOVER STRIPS 
one step wart remover plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72446-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 mg  in 14

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72446-008-14	14 in 1 BOX; Type 0: Not a Combination Product	09/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	09/01/2018

Labeler - Hudson Health LLC (081276171)