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Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer (Fikes Northwest, Corp.)

Available Formats

Dosage Form Package Information Links
SOLUTION 3785 mL in 1 BOTTLE (50036-514-05) Label Information

Complete Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer Information

  • 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 eyes 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


  • Principal Display Panel

    Fikes Northwest

    Non AlcoholFoaming 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

    Package Label

  • INGREDIENTS AND APPEARANCE
    FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER 
    husky 514 solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50036-514
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride 1 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50036-514-05 3785 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333 11/16/2009
    Labeler - Fikes Northwest, Corp. (167376284)
    Registrant - Fikes Northwest, Corp. (167376284)
    Establishment
    Name Address ID/FEI Business Operations
    Canberra Corporation 068080621 MANUFACTURE