CORNEX- corn and callus liquid remover liquid

Cornex by

Drug Labeling and Warnings

Cornex 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 17%w/w

Purpose

Corn and callus remover

Uses

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

​ ​Warnings

For external use only.​

Flammable

• keep away from fire or flame
• cap bottle tightly and store at room temperature away heat

Do not use 

• on irritated skin
• on any area that is infected or reddened
• if you are a diabetic, or if you have poort blood circulation, excpet under the advice and supervision of a doctor or podiatrist

When using this product

• avoid contact with eyes
• avoid inhaling vapors
• if product gets into the eyes, flush with water for 15 minutes

Stop and ask a 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 thoroughly
• apply one drop at a time with applicator, to sufficiently cover each corn/callus; let dry
• use cushions with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
• repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

Other information

• store between 20°C to 30°C (68°F to 86°F)
• clsoe tightly to prevent solidification 
• store in a cool place

Inactive ingredients

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

Principal Display Panel

Premier

Liquid Corn & Callus Remover

Salicylic Acid

Safely removes corn & calluses

Soft foam cushions and protects

3 CUSHIONS 0.33 FL OZ (9.8 mL)

INGREDIENTS AND APPEARANCE

CORNEX 
corn and callus liquid remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.17 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PYROXYLIN (UNII: KYR8BR2X6O)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CASTOR OIL (UNII: D5340Y2I9G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-009-15	15 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2013	10/10/2015
2	NDC: 56104-009-09	9 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	10/10/2015

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)