Label: MG DERMACLEAN- n/a liquid

  • NDC Code(s): 50241-014-01, 50241-014-02
  • Packager: Morgan Gallacher Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated December 21, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Benzalkonium Chloride........0.13%

  • Uses

    • For Hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
  • Purpsoe

    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.

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

  • Directions

    • Apply small amount of product to wet hands
    • Work into lather and rinse thoroughly
    • Dry hands
  • Inactive Ingredients

    • cocamidopropyl betaine
    • disodium cocoamphodipropionate
    • glycerin
    • lauramine oxide
    • magnesium nitrate
    • methylchloroisothiazolinone
    • methylisothiazolinone
    • sodium chloride 
    • water
  • MG DermaClean 

    image description
  • INGREDIENTS AND APPEARANCE
    MG DERMACLEAN 
    n/a liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50241-014-021 in 1 BOX01/25/2019
    1NDC:50241-014-013756 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/25/2019
    Labeler - Morgan Gallacher Inc. (028311595)
    Registrant - Morgan Gallacher Inc. (028311595)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morgan Gallacher Inc.028311595manufacture(50241-014) , api manufacture(50241-014) , pack(50241-014)