Label: HAND SANITIZER- benzalkonium chloride 0.1%w/w liquid

  • NDC Code(s): 54622-148-20
  • Packager: Georgia Pacific Consumer Products
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 18, 2024

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  • Claims

    enMotion

    Foam Hand Sanitizer

    with Moisturizers

    Alcohol Free

    Fregrance Free   SKU 42338

  • Active ingredients

    Benzalkonium Chloride 0.1% w/w

  • Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on skin that could cause disease
    • Recommended for repeated use
  • Warnings

    for external use only

  • When using this product

    do not use in or near eyes

  • Discontinue use

    If irritation or redness develops.  If condition persists for more than 72 hours, consult a pysician

  • Keep out of reach of children

    If swallowed, seek medical attention or call a poison control center immediately.

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping.
  • Inactive ingredients

    water, decyl glucoside, PEG-12 Dimethicone, Aloe Barbadensis Leaf Juice, Propylene Gycol, Glycerin, Panthenol Dipotassium Phosphate, Potassium Phosphate

  • Adverse Reaction

    Manufacture for

    Georgia-Pacific Consumer Products LP. Altanta, GA 30303

    Questions? Call 1-866-HELLOGP (435-5647)

    or visit us online at www.gppro.com

    2017 Georgia-Pacific Consumer Products LP All rights reserved

  • Principal display panel

    Foam Hand Sanitizer

    with Moisturizers

    Alcohol Free

    1000 mL (33.8 FL OZ)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    benzalkonium chloride 0.1%w/w liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-148
    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
    WATER (UNII: 059QF0KO0R)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)  
    POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-148-201000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/01/2017
    Labeler - Georgia Pacific Consumer Products (806142217)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(54622-148)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(54622-148)
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