SALICYLIC ACID- medicated corn removers patch

Salicylic acid by

Drug Labeling and Warnings

Salicylic acid by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Salicylic acid 40%

Purpose

Corn remover

Uses

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

Warnings

For external use only.

Do not use

• if you are diabetic
• if you 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
• if necessary, cut medicated patch to fit corn
• apply adhesive side of medicated patch onto corn
• cover medicated patch with pad
• after 48 hours, remove medicated patch
• repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
• may soak corn in warm water for 5 minutes to assist in removal

Other Information

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

Inactive Ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

1-888-287-1915

Principal Display Panel

equate

Medicated

Corn

Removers

Salicylic Acid 40%

• Effective corn removal treatment
• Cushions against pressure & friction

9 Medicated Patches/9 Pads

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
medicated corn removers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-155
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 9

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-155-09	9 in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	03/15/2019

Labeler - Wal-Mart Stores Inc (051957769)

Registrant - Premier Brands of America Inc. (063849780)