Label: D-FENZ HAND SANITIZER- benzalkonium chloride liquid

  • Contains inactivated NDC Code(s)
    NDC Code(s):     73733-100-02, 73733-100-03, 73733-100-04, 73733-100-05, view more
    73733-100-06, 73733-100-07, 73733-100-10, 73733-100-13, 73733-100-14, 73733-100-20, 73733-100-21, 73733-100-22, 73733-100-23, 73733-100-24, 73733-100-30, 73733-100-31, 73733-100-32
  • Packager: N2N Global, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 14, 2022

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  • Active Ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    Skin Antiseptic

  • Uses

    For hand and skin sanitizing to decrease microbes on skin

  • Warnings

    For external use only. Do not use in the eyes. In case of eye contact, flush thoroughly with water & seek medical attention.

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

  • Keep out of reach of children

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

  • Directions

    Dispense an adequate amount in palm to cover hands. Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product.

  • Other Information

    Skin cells may be shed naturally or by abrasion prior to 4 hours, exposing fresh, unprotected skin. Reapply as needed.

  • Inactive Ingredients

    Colloidal Silicon Dioxide

  • Questions?

    inquiries@N2Ncleangreen.com

    www.n2ncleangreen.com

    N2N Global, LLC

    2011 West Danforth Rd #162

    Edmond, OK 73003

  • D-FENZ HAND SANITIZER

    D-FENZ-Hand-Sanitizer

  • INGREDIENTS AND APPEARANCE
    D-FENZ HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73733-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 0.2 g  in 100 mL
    WATER (UNII: 059QF0KO0R) 99.67 g  in 100 mL
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73733-100-02125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/17/2020
    2NDC:73733-100-03250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/17/2020
    3NDC:73733-100-041000 mL in 1 BAG; Type 0: Not a Combination Product03/17/2020
    4NDC:73733-100-053785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/17/2020
    5NDC:73733-100-13500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/17/2020
    6NDC:73733-100-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    7NDC:73733-100-1410 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/17/2020
    8NDC:73733-100-0659 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    9NDC:73733-100-07473 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    10NDC:73733-100-201249050 mL in 1 CONTAINER; Type 0: Not a Combination Product03/17/2020
    11NDC:73733-100-2118925000 mL in 1 TANK; Type 0: Not a Combination Product03/17/2020
    12NDC:73733-100-30100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/17/2020
    13NDC:73733-100-2259 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/17/2020
    14NDC:73733-100-23208198 mL in 1 DRUM; Type 0: Not a Combination Product03/17/2020
    15NDC:73733-100-241041000 mL in 1 CONTAINER; Type 0: Not a Combination Product03/17/2020
    16NDC:73733-100-31236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/17/2020
    17NDC:73733-100-32236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/17/2020
    Labeler - N2N Global, LLC (117570307)
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