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Native Green Foaming Hand Sanitizer (Native Green)

Available Formats

Dosage Form Package Information Links
SOLUTION 550 mL in 1 BOTTLE (50409-514-82) Label Information
SOLUTION 50 mL in 1 BOTTLE (50409-514-42) Label Information

Complete Native Green Foaming Hand Sanitizer Information

  • Active Ingredient:

    Benzalkonium Chloride 0.1%


  • Purpose

    Antimicrobial


  • Uses

    • For hand sanitizing to decrease bacteria on the skin

  • 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 – Bottle Label

    NATIVE GREEN
    FOAMING HAND SANITIZER
    ALCOHOL-FREE – WITH MOISTURIZERS

    Cleaner, Greener

    SEE SIDE PANEL FOR ADDITIONAL INFORMATION.

    Principal Display Panel – Bottle Label

  • INGREDIENTS AND APPEARANCE
    NATIVE GREEN FOAMING HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50409-514
    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:50409-514-82 550 mL in 1 BOTTLE
    2 NDC:50409-514-42 50 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333 04/21/2010
    Labeler - Native Green (791610038)
    Establishment
    Name Address ID/FEI Business Operations
    Canberra Corporation 068080621 MANUFACTURE