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 Chain Drug Consortium, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active ingredient

Salicylic acid

​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
• have poor blood circulation
• on irritated skin, or any area that is infected or reddened

Ask your doctor

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 area 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 5 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 1-866-964-0939

Principal Display Panel

​Premier Value​

Medicated Corn Removers

Salicylic acid

• Therapeautic corn removal treatment
• Protects against pressure & pain

9 Medicated Patches/9Pads

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
medicated corn removers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-606
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 (UNII: 532B59J990)
VINYL ACETATE (UNII: L9MK238N77)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-606-00	9 in 1 PACKAGE; Type 0: Not a Combination Product	05/23/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	05/23/2003

Labeler - Chain Drug Consortium, LLC (101668460)