Label: MG DERMAGEL 70- ethyl alcohol liquid

  • NDC Code(s): 50241-465-02, 50241-465-04
  • Packager: Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active Ingredient

    Ethyl Alcohol....70%

  • Purpose

    Antimicrobial

  • Uses

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

    • For external use only.
    • Flammable keep away from fire or flame
  • When using this product

    • Avoid contact with eyes. In case of eye contract, flush eyes with water. 
  • Stop use and ask doctor if

    • irritation or redness develops, if condition persists for more than 72 hours.  
  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Conrol Center right away

  • Directions

    • Place a small amount of MG Dermagel 70 in your palm to throughly cover your hands. 
    • Rub hands together briskly until dry. 
    • Keep out of reach of children.  For children under 6, use only under adult supervison.  Not recommended for infants.  
  • Inactive Ingredients

    • Water
    • Isopropyl Alcohol
    • Glycerin
    • Propylene Glycol
    • Carbomer
    • Triisopropanolamine
  • MG DermaGel 70

    MG DermaGel 70image description

  • INGREDIENTS AND APPEARANCE
    MG DERMAGEL 70 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-465
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 L  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)  
    CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50241-465-02208.198 L in 1 DRUM; Type 0: Not a Combination Product02/01/2024
    2NDC:50241-465-043.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02/01/2024
    Labeler - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
    Registrant - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.028311595manufacture(50241-465) , api manufacture(50241-465) , pack(50241-465)
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