Label: ALASKA AIRLINES- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • Warnings:

    For external use only.

    Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
    Stop use and ask a doctor if skin irritation develops.
    If ingested, get medical help or contact a Poison Control Center immediately.

    Warnings:

    Keep out of reach of children.

  • Directions:

    Liberally apply product to skin by gently massaging until absorbed.
    Supervise children in the use of this product.

  • Uses:

    To decrease bacteria on the skin.

  • Purpose:

    Antibacterial.

  • Drug facts:

    Active Ingredients: Benzalkonium Chloride.

  • Inactive Ingredients:

    Water (Aqua), Glycerin, PEG-40 Hydrogenated Castor Oil, DMDM Hydantoin, Propylene Glycol, Parfum, Aloe Barbadensis Leaf Extract

  • Other Information:

    Avoid extreme temperatures.

  • Alaska Arilines Foam Hand Sanitizer

    Alaska Alcohol Free Hand Sanitizer

    Alaska hand Sanitizer

    Hand Sanitizer
    Ocean Citron

    This is a pump item with no dosage information. Most customers use 1-2 pumps.

  • INGREDIENTS AND APPEARANCE
    ALASKA AIRLINES 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52305-602
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE (UNII: AUG1H506LY) 0.5 g  in 100 mL
    WATER (UNII: 059QF0KO0R) 97.05 g  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 g  in 100 mL
    DMDM HYDANTOIN (UNII: BYR0546TOW) 0.2 g  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 3 g  in 100 mL
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) 0.75 g  in 100 mL
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52305-602-30250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/29/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/29/2020
    Labeler - Freshorize Ltd. (424168503)
    Registrant - Freshorize LLC (018206924)
    Establishment
    NameAddressID/FEIBusiness Operations
    China Ningbo Shangge Cosmetic Technology Corp.529287434manufacture(52305-602)
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