NDC 56104-009

Cornex

Corn And Callus Liquid Remover

Cornex is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Premier Brands Of America Inc.. The primary component is Salicylic Acid.

• Product ID: 56104-009_53dd77c7-0eab-4000-8865-402a361cc662
• NDC: 56104-009
• Product Type: Human Otc Drug
• Proprietary Name: Cornex
• Generic Name: Corn And Callus Liquid Remover
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-01-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part358F
• Labeler Name: Premier Brands of America Inc.
• Substance Name: SALICYLIC ACID
• Active Ingredient Strength: 0 g/g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 56104-009-09

9 g in 1 BOTTLE, WITH APPLICATOR (56104-009-09)

• Marketing Start Date: 2015-10-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 56104-009-09 [56104000909]

Cornex LIQUID

• Marketing Category: OTC monograph final
• Application Number: part358F
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-10-10

NDC 56104-009-15 [56104000915]

Cornex LIQUID

• Marketing Category: OTC monograph final
• Application Number: part358F
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-01
• Marketing End Date: 2015-10-10

Drug Details

Active Ingredients

Ingredient	Strength
SALICYLIC ACID	.17 g/g

OpenFDA Data

• SPL SET ID: 4f0b5582-80e6-432b-afd3-de251b6b2451
• Manufacturer:
  • Premier Brands of America Inc.
• UNII:
  • O414PZ4LPZ
• RxNorm Concept Unique ID - RxCUI:
  • 312881

NDC Crossover Matching brand name "Cornex" or generic name "Corn And Callus Liquid Remover"

NDC	Brand Name	Generic Name
56104-009	Cornex	Corn and Callus Liquid Remover
82160-238	Cornex	Lactic Acid, Salicylic Acid