SALICYLIC ACID- one-step corn remover clear patch

Salicylic Acid by

Drug Labeling and Warnings

Salicylic Acid by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 40%w/w

​Purpose

Corn remover

​Use

• for the removal of corns

​Warnings

For external use only.

Do not use

• if you are a diabetic
• 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: may soak corn in warm water for 5 minutes to assist in removal

• dry area thoroughly

• remove bandage strips by peeling backing off at slit

• adhere medicated strip directly over corn

• after 48 hours remove medicated bandage strip

• repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

​Other information

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

Inactive ingredients

acrylic adhesive, brown iron oxide, polyethylene foam

Questions?

call 1-866-964-0939

​Principal Display Panel

Premier

One-Step Clear

Corn Removers

Medicated

Salicylic acid

• Maximum strength
• Cushions, conceals and protects while removing corns
• No messy liquids

6 Medicated One-Step Clear Bandages

INGREDIENTS AND APPEARANCE

SALICYLIC ACID 
one-step corn remover clear patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-021
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 6

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
BROWN IRON OXIDE (UNII: 1N032N7MFO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-021-06	6 in 1 BOX; Type 0: Not a Combination Product	01/01/2013

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

Labeler - Premier Brands of America Inc. (080051232)

Registrant - Premier Brands of America Inc. (063849780)

Establishment
Name	Address	ID/FEI	Business Operations
Premier Brands of America Inc.		080051232	relabel(56104-021) , repack(56104-021)