MEDICATED CALLUS REMOVERS- salicylic acid patch

Drug Labeling and Warnings

Drug Details [pdf]

​Active ingredient

Salicylic acid 40%

Purpose

Callus remover

Uses

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

Warnings

For external use only.

Do not use

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

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 and dry thoroughly
• if necessary, cut medicated patch to fit callus
• carefully adhere medicated patch direclty over callus
• cover medicated patch with pad
• after 48 hours, remove medicated patch
• 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° to 30°C (59°F and 86°F)
• avoid surrounding skin when applying medicated patch

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-866-964-0939

Principal Display Panel

premier
solutions

Medicated
CALLUS
REMOVERS

SALICYLIC ACID 40% / CALLUS REMOVER

MAXIMUM STRENGTH
Effective callus removal treatment
Protects against pressure & friction

6 Pads

4 Medicated Patches

INGREDIENTS AND APPEARANCE

MEDICATED CALLUS REMOVERS 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-913
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
POLYVINYL ALCOHOL (UNII: 532B59J990)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-913-01	4 in 1 BOX	05/22/2026
1		1 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	05/22/2026

Labeler - Premier Brands of America Inc (063849780)