NDC 50241-013

MG DermaSan

Mg Dermasan

MG DermaSan is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Morgan Gallacher Inc.. The primary component is Benzalkonium Chloride.

• Product ID: 50241-013_b200936f-f7b2-463c-a6b5-07a71e53878a
• NDC: 50241-013
• Product Type: Human Otc Drug
• Proprietary Name: MG DermaSan
• Generic Name: Mg Dermasan
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-12-03
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333E
• Labeler Name: Morgan Gallacher Inc.
• Substance Name: BENZALKONIUM CHLORIDE
• Active Ingredient Strength: 0 g/100g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50241-013-01

3756 g in 1 BOTTLE, PLASTIC (50241-013-01)

• Marketing Start Date: 2013-12-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50241-013-01 [50241001301]

MG DermaSan LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part333E
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-12-03
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
BENZALKONIUM CHLORIDE	.13 g/100g

OpenFDA Data

• SPL SET ID: 8e10860e-b936-4693-a46c-c13624204316
• Manufacturer:
  • Morgan Gallacher Inc.
• UNII:
  • F5UM2KM3W7
• RxNorm Concept Unique ID - RxCUI:
  • 1046593

NDC Crossover Matching brand name "MG DermaSan" or generic name "Mg Dermasan"

NDC	Brand Name	Generic Name
50241-013	MG DermaSan	MG DermaSan
50241-259	MG DermaSan	N/A
76533-010	MG DermaSan	Benzalkonium Chloride Foaming Hand Sanitizer