SCOTT CLEAR CORN REMOVERS- 40% w/w salicylic acid corn remover plaster

Scott Clear Corn Removers by

Drug Labeling and Warnings

Scott Clear Corn Removers by is a Otc medication manufactured, distributed, or labeled by Creative Foam Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 40% w/w

Purpose

Corn Removal

Uses

• For removal of corns
• Relieves pain by removing corns

Warning

For external use only

Do not use:

• If you are a diabetic
• If you have poor blood circulation
• On irritated skin or area that is infected or reddened

STOP USE

Stop use and ask a doctor if discomfort lasts

Keep out of reach of children

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center immediately.

Directions:

Wash affected area, dry thoroughly
If necessary, cut medicated disk to fit corn
Apply medicated disk with sitcky side adhereing to skin
Cover medicated disk with enclosed cushion
After 48 hours, remove disk
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 a

Other Information

Store between 15 o C and 30 o C (59 o F and 86 o F)

Inactive Ingredients

Vinyl Acetate

Scott Clear Corn Removers

INGREDIENTS AND APPEARANCE

SCOTT CLEAR CORN REMOVERS 
40% w/w salicylic acid corn remover plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82660-006
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, UNSPECIFIED (UNII: 532B59J990)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82660-006-05	100 mg in 1 BOX; Type 0: Not a Combination Product	12/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	12/31/2020

Labeler - Creative Foam Corporation (620897061)