SALICYLIC ACID- hydrogel clear wart remover patch

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. 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

• if you are a diabetic
• if you have poor blood circulation
• 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

Stop use and ask a 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
• if necessary, cut medicated disc to fit wart
• apply adhesive side down of disc onto wart
• cover disc with cushions to conceal area
• repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

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

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

Call 1-866-964-0939

Principal Display Panel

CVS Health

Hydrogel

Clear

Wart

Remover

SALICYLIC ACID 40%

MAXIMUM

STRENGTH

• Maximum strength salicylic acid

removes warts safely & effectively

• Cushions & conceals
• Thin, flexible bandage

provides contoured fit

9 CUSHIONS

12 MEDICATED DISCS

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
hydrogel clear wart remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-294
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 12

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
VINYL ACETATE (UNII: L9MK238N77)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-294-09	12 in 1 PACKAGE; Type 0: Not a Combination Product	02/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	02/01/2020

Labeler - CVS Pharmacy (062312574)