Label: MG DERMASAN- n/a liquid

  • NDC Code(s): 50241-259-01, 50241-259-02
  • Packager: Morgan Gallacher Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active Ingredient

    Benzalkonium Chloride.........0.1 %

  • Uses

    • For hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
  • Purpose

    Antimicrobial

  • Warnings

    • For external use only.
    • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.
    • Stop use and ask a doctor if irritation or redness develops and conditions persist.
  • Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Conrol Center right away

  • Directions

    • Pump a small amount of foam into palm of hand.
    • Rub thoroughly over all surfaces of both hands.
    • Rub hands together briskly until dry.
  • Inert Ingredients

    • water
    • cetrimonium chloride
    • laurtrimonium chloride
    • dihydroxyethyl cocamine oxide
    • glycereth-17 cocoate
    • citric acid
  • MG DermaSan

    MG DermaSanimage description

  • INGREDIENTS AND APPEARANCE
    MG DERMASAN 
    n/a liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-259
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50241-259-021 in 1 BOX10/01/2018
    1NDC:50241-259-013756 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM10/01/2018
    Labeler - Morgan Gallacher Inc. (028311595)
    Registrant - Morgan Gallacher Inc. (028311595)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morgan Gallacher Inc.028311595manufacture(50241-259) , api manufacture(50241-259) , pack(50241-259)
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