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 Hudson Health LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%

Purpose

Callus remover

Use

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

Warnings

For external use only.

Do not use

• if you are a 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 patch to fit corn
• apply adhesive side down 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 15 minutes to assist in removal

Other information

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

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-877-237-0194

Principal Display Panel

comfortzone

medicated

corn removers

salicylic acid

• effective corn removal treatment
• cushions against pressure & friction

18 pads/ 18 medicated patches

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
medicated corn removers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72446-002
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 18

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: 72446-002-18	18 in 1 PACKAGE; Type 0: Not a Combination Product	08/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	08/31/2018

Labeler - Hudson Health LLC (081276171)