SALICYLIC ACID- medicated callus removers patch

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association. Drug facts, warnings, and ingredients follow.

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°C to 30°C (59°F to 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

QC

Quality Choice

Medicated

Callus

Removers

Salicylic Acid 40% / Callus Remover

Effective Callus Removal Treatment

Protects Against Pressure & Friction

6 Pads

4 Medicated Patches

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
medicated callus removers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-230
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
VINYL ACETATE (UNII: L9MK238N77)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
POLYVINYL ALCOHOL (UNII: 532B59J990)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-230-04	4 g in 1 CARTON; Type 0: Not a Combination Product	04/25/2025	05/06/2025
2	NDC: 83324-230-01	4 in 1 BOX	04/14/2025
2		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	04/14/2025

Labeler - Chain Drug Marketing Association (011920774)