Label: MG DERMAWASH- benzalkonium chloride liquid

  • NDC Code(s): 50241-302-01, 50241-302-02, 50241-302-03
  • Packager: Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Updated December 21, 2023

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  • ACTIVE INGREDIENT

    Benzalkonium Chloride......0.13%

  • 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.

    -  Do not ingest. Stop use and contact a doctor if irritation or

        redness develop or conditions persist.

  • Keep out of reach of children.

    If swallowed, get medical help

    or contact Poison Control Center right away. 

  • Directions

    - Apply small amount of product to wet hands.

    - Work into lather and rinse thogoughly. Dry hands.

  • INERT INGREDIENTS:

    Aloe Barbadensis Leaf Juice, Caprylyl/Capryl Gluciside, Citric Acid, Cocamide MIPA, Cocamidopropyl Betaine, Glycerin, Lauryl Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchloroisothiazolinone, Methylthiazolinone, PEG
    150 Distearate, Tetrasodium EDTA, Water

  • MG DermaWash

    image description
  • INGREDIENTS AND APPEARANCE
    MG DERMAWASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-302
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 kg  in 100 kg
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA FLOWER (UNII: 575DY8C1ER)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50241-302-021 in 1 BOX09/24/2018
    1NDC:50241-302-013.80564 kg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:50241-302-03210.25 kg in 1 DRUM; Type 0: Not a Combination Product09/24/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/24/2018
    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(50241-302) , api manufacture(50241-302) , pack(50241-302)
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