Label: BITTOL ANTI-BACTERIAL HYGIENIC HAND CLEANING LIQUID- benzalkonium chloride liquid

  • NDC Code(s): 78564-003-01, 78564-003-02
  • Packager: Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 15, 2023

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  • Drug Facts

  • Active Ingredients

    Benzalkonium Chloride 0.1%

    Purpose

    Antibacterial

  • Uses

    • To decrease bacteria on the skin.
    • When water, soap & towel are not available.
    • Recommended for repeated use
  • WARNINGS

    For external use only.

    Flammable, keep away from fire or flame

    When using this product:

    Do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if:

    Irritation and redness develops and last more than 72 hours.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

  • Directions:

    Remove all your jewelry before use. Be careful to there is no visible dirtiness on the hands and make should that hands and skin not wet. Take 3-5 ml of Bittol Antibacterial Hygienic Hand Cleaning Liquid. Rub hands until it is dry properly.

  • Other Information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces.
  • Inactive Ingredients:

    Aqus/Water, Isopropyl Alcohol, Glycerin.

  • Package Labeling:1000ml

    Box

  • Package Labeling:750ml

    Box2

  • INGREDIENTS AND APPEARANCE
    BITTOL ANTI-BACTERIAL HYGIENIC HAND CLEANING LIQUID 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78564-003
    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)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78564-003-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/2020
    2NDC:78564-003-02750 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/20/2020
    Labeler - Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Limited Sirketi (565657236)
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