Label: ALASKA AIRLINES- benzalkonium chloride liquid

  • 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 October 3, 2022

If you are a consumer or patient please visit this version.

  • 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 not finalpart333A06/29/2020
    Labeler - Freshorize Ltd. (424168503)
    Registrant - Freshorize LLC (018206924)
    Establishment
    NameAddressID/FEIBusiness Operations
    China Ningbo Shangge Cosmetic Technology Corp.529287434manufacture(52305-602)