Label: MG FOAMSAN 70- ethyl alcohol liquid

  • NDC Code(s): 50241-223-02, 50241-223-03
  • 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 ...........70.0% v/v

  • Purpose

    Antiseptic

  • Uses

    For hand sanitizing to decrease bacteria on the skin.

    recommended for repeated use.

  • Warnings

    For external use only.

  • When Using this Product

    - Avoid contact with eyes.

    - In case of eye contact, flush eyes with water.

  • Stop use and ask a doctor if

    -Irritation or redness develops, if condition persists for more than 72 hours. 

  • Keep out of reach of children.

    Keep out of reach of children. If swallowed, get medical help

    or contact a Poison Control Center immediately.

  • Directions

    -Pump a small amount of foam into palm of hand.  

    -Rub thoroughly over all surfaces of both hands.  

    -Rub hands together brisky until dry

    -Use between hand washings to help reduce germ tranmission 

  • Inactive Ingredients

    Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Glycerin, Isopropyl Alcohol, Perfluorohexylethyl Alcohol, Water.

  • MG FoamSan 70

    MG FoamSan 70image description

  • INGREDIENTS AND APPEARANCE
    MG FOAMSAN 70 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-223
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 L  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50241-223-023.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/21/2020
    2NDC:50241-223-03208.198 L in 1 DRUM; Type 0: Not a Combination Product08/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM08/21/2020
    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(50241-223) , api manufacture(50241-223) , pack(50241-223)
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