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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC: 76533-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76533-010-070.207 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/22/202006/26/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/20/202006/26/2021
Labeler - US Continental (793141912)
Establishment
NameAddressID/FEIBusiness Operations
US Continental793141912manufacture(76533-010)

Revised: 6/2021
 

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