Label: HUSKY 514 NON-ALCOHOL FOAMING INSTANT HAND SANITIZER- husky 514 solution

  • 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 November 3, 2009

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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
  • Warning

    For external use only

    When using this product avoid contact with eyes. In case of eye contact, flush with water.

    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

    • 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, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2, cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

    Manufactured By:
    CANBERRA CORPORATION
    3610 Holland-Sylvania Rd.
    Toledo, Ohio 43615

  • PRINCIPAL DISPLAY PANEL

    Label Content for 128 Fl. Oz:

    Husky®

    514

    NON-ALCOHOL FOAMING INSTANT HAND SANITIZER

    • Enhanced with Moisturizers
    • Kills disease causing germs within seconds
    • Effective against MRSA, VRE, E. coli (0157:H7), Staphylococcus, Streptococcus and other organisms
    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    See side panel for additional information.

    For Hospital And Professional Use Only

    Net Contents: One gallon (128 Fl. Oz.) 3.78 liters

    Label Content for 128 Fl. Oz
  • PRINCIPAL DISPLAY PANEL

    Label Content for 18.60 Fl. Oz:

    Husky®

    514

    NON-ALCOHOL FOAMING INSTANT HAND SANITIZER

    • Enhanced with Moisturizers

    • Kills disease causing germs within seconds

    • Effective against MRSA, VRE, E. coli (0157:H7), Staphylococcus, Streptococcus and other organisms

    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    See side panel for additional information.

    For Hospital And Professional Use Only

    Net Contents: 18.60 fl. oz./550 mL.

    Label Content for 18.60 Fl. Oz
  • PRINCIPAL DISPLAY PANEL

    Label Content for 250 mL:

    Husky

    514

    NON-ALCOHOL FOAMING INSTANT HAND SANITIZER

    • Enhanced with Moisturizers

    • Kills disease causing germs within seconds

    • Effective against MRSA, VRE, E. coli (0157:H7), Staphylococcus, Streptococcus and other organisms

    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    See side panel for additional information.

    For Hospital And Professional Use Only

    Net Contents: 250 mL

    514-001-001-S01F

    Label Content for 250 mL
  • PRINCIPAL DISPLAY PANEL

    Label Content for 1.69 Fl Oz:

    Husky

    514

    NON-ALCOHOL FOAMING INSTANT HAND SANITIZER

    • Enhanced with Moisturizers

    • Kills disease causing germs within seconds

    • Effective against MRSA, VRE, E. coli (0157:H7), Staphylococcus, Streptococcus and other organisms

    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    See side panel for additional information.

    For Hospital And Professional Use Only

    Net Contents: 1.69 fl. Oz (50 mL)

    Label Content for 1.69 Fl Oz
  • INGREDIENTS AND APPEARANCE
    HUSKY 514 NON-ALCOHOL FOAMING INSTANT HAND SANITIZER 
    husky 514 solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-514
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride1 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    dihydroxypropyl peg-5 linoleammonium chloride (UNII: 0Y0NQR2GH1)  
    glycereth-2 cocoate (UNII: JWM00VS7HC)  
    behentrimonium chloride (UNII: X7GNG3S47T)  
    dihydroxyethyl cocamine oxide (UNII: 8AR51R3BL5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63779-514-103785 mL in 1 BOTTLE
    2NDC:63779-514-82550 mL in 1 BOTTLE
    3NDC:63779-514-99250 mL in 1 BOTTLE
    4NDC:63779-514-4250 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33311/16/2009
    Labeler - Canberra Corporation (068080621)
    Registrant - Canberra Corporation (068080621)
    Establishment
    NameAddressID/FEIBusiness Operations
    Canberra Corporation068080621MANUFACTURE
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