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
  • 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 February 3, 2023

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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 not finalpart333A12/01/2017
    Labeler - Georgia Pacific Consumer Products (806142217)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(54622-148)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(54622-148)
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