MG DermaSan 7 ounce Foaming Hand Sanitizer

MG DermaSan by

Drug Labeling and Warnings

MG DermaSan by is a Otc medication manufactured, distributed, or labeled by US Continental. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MG DERMASAN 07- benzalkonium chloride foaming hand sanitizer liquid 
US Continental

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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MG DermaSan 7 ounce Foaming Hand Sanitizer

MG DermaSan 7 oz Foaming Hand Sanitizer

MG DermaSan 7 oz Foaming Hand Sanitizer
NDC: 76533-010-07 207 mL

MG DermaSan Foaming Hand Sanitizer 207 mL

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitzer 7 ounce

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

76533-010-07 207mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

76533-010-07 237mL

MG DermaSan Foaming Hand Sanitizer 7 ounce

MG DERMASAN  07
benzalkonium chloride foaming hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76533-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76533-010-07	0.207 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/22/2020	06/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/20/2020	06/26/2021

Labeler - US Continental (793141912)

Establishment
Name	Address	ID/FEI	Business Operations
US Continental		793141912	manufacture(76533-010)

Revised: 6/2021

Document Id: c5ad16c8-8127-88c4-e053-2a95a90a9d64

34390-5

Set id: a641302f-7230-d850-e053-2a95a90a5e46

Version: 2

Effective Time: 20210626