MEDICATED CALLUS REMOVERS EXTRA THICK- salicylic acid patch

Medicated Callus Removers Extra Thick by

Drug Labeling and Warnings

Medicated Callus Removers Extra Thick by is a Otc medication manufactured, distributed, or labeled by Meijer Distribution Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%

Purpose

Callus remover

Use

• 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, 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 area thoroughly
• if necessary, cut medicated patch to fit callus
• apply adhesive side of medicated patch onto callus
• cover medicated patch with pad
• after 48 hours, remove medicated patch
• repeat 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° and 30°C (59° 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

meijer

Extra Thick

callus

removers

Salicylic Acid 40%/Callus Remover

Effective callus removal treatment

Extra thick pads protect against friction & reduce pressure

4 Pads | 4 Medicated Patches

INGREDIENTS AND APPEARANCE

MEDICATED CALLUS REMOVERS EXTRA THICK 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79481-0611
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
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: 79481-0611-1	4 in 1 CARTON	08/23/2023
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	01/01/2017

Labeler - Meijer Distribution Inc (006959555)