Label: CORNEX- corn and callus liquid remover liquid
- NDC Code(s): 56104-009-09, 56104-009-15
- Packager: Premier Brands of America Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
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
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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
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
CORNEX
corn and callus liquid remover liquidProduct 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 Drug M030 01/01/2013 Labeler - Premier Brands of America Inc. (117557458)