EXTRA THICK CALLUS REMOVERS- extra thick callus removers with salicylic acid patch

Extra Thick Callus Removers by

Drug Labeling and Warnings

Extra Thick Callus Removers by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores, Inc.. 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 diabetic
• if you have poor blood circulation
• on irritated skin or any area that is infected or reddened

​If discomfort persists

see your doctor or podiatrist

​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 patches to fit callus
• apply the adhesive side down 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 59° and 86°F (15° and 30°C)

​Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

​Questions?

call 1-888-287-1915

Principal Display Panel

Equate

Extra Thick Callus Removers

Salicylic Acid 40%

• Effective callus removal treatment
• Extra thick pads protect against friction and reduce pressure

4 Medicated Patches/ 4 Pads

INGREDIENTS AND APPEARANCE

EXTRA THICK CALLUS REMOVERS 
extra thick callus removers with salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-019
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 100 mg

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-019-04	160 mg in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	08/01/2013

Labeler - Wal-Mart Stores, Inc. (051957769)