Label: DECON7 ANTISEPTIC FOAMING HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 78245-201-01, 78245-201-03, 78245-201-04, 78245-201-05, view more
    78245-201-06
  • Packager: Decon7 Systems, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 16, 2023

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  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • 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 thoroughly with water.

    Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control 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
  • Inactive Ingredients

    Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid

  • PRINCIPAL DISPLAY PANEL

    Decon7 Antiseptic Foaming Hand Sanitizer
    Manufactured for: D7™ DECON SEVEN

    110 North Freeport Parkway, Suite 120, Coppell, TX 75019

    1.844.727.FOAM (North America)

    +1.469.830.1800 (International) | info@decon7.com

    1.7 fl oz (50 mL)

    24/7 Emergency Response, Contact Chemtrec

    800-424-9300 (North America)

    +1-703-527-3887 (International)

    50 mL

    550 mL

    1000 mL

  • INGREDIENTS AND APPEARANCE
    DECON7 ANTISEPTIC FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78245-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78245-201-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/2021
    2NDC:78245-201-03550 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/2021
    3NDC:78245-201-053800 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/2021
    4NDC:78245-201-041000 mL in 1 BAG; Type 0: Not a Combination Product11/22/202106/30/2023
    5NDC:78245-201-061041000 mL in 1 CONTAINER; Type 0: Not a Combination Product11/22/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/22/2021
    Labeler - Decon7 Systems, LLC (079281162)
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