SALICYLIC ACID- gel callus 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%

Purpose

Callus Remover

Uses

• for the removal of calluses
• releves pain by removing calluses

Warnings

For external use only.

Do not use

• if you are a diabetic
• have poor blood circulation
• on irritated skin, on any area that is infected or reddened

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 and dry thoroughly
• apply adhesive side down of medicated disc on to the callus
• cover the medicated disc with gel cushion
• after 48 hours, remove medicated disc
• repeat this procedure every 48 hours as needed for up to 14 days (until callus is removed)
• may soak callus in warm water for 5 minutes to assist in removal

Other information

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

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-866-964-0939

Principal Display Panel

CVS Health

Medicated

Gel Callus Removers

SALICYLIC ACID 40%

• Maximum strength salicylic acid removes calluses safely & effectively
• Cushions & conceals
• Thin & flexible to fit inside shoes

4 CUSHIONS

4 MEDICATED DISCS

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
gel callus remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-202
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 4

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-202-04	4 in 1 PACKAGE; Type 0: Not a Combination Product	07/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	07/31/2018

Labeler - CVS Pharmacy (062312574)