Label: BENZALKONIUM CHLORIDE- liquid hand soap liquid

  • NDC Code(s): 72288-021-32
  • Packager: AMAZON.COM SERVICES LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 20, 2026

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

  • Active Ingredient

    Benzalkonium Chloride (0.13%)

  • Purpose

    Antibacterial.

  • Uses

    For hand washing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    When using this product

    • Avoid contact with eyes. In case of contact, rinse throughly with water.

    Stop use and ask a doctor if

    • Irritaion or redness develops and lasts 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

    • Use to refil a foaming hand soap pump bottle.
    • Apply onto dry hands. Lather and rinse thoroghly with water,
  • Inactive Ingredients.

    Water (Aqua), Cocamidopropyl Betaine, Glycerin, Fragrance (Parfum), Polysorbate 20, Tetrasodium EDTA, Hydroxyethylcellulose, Decyl Glucoside, Citric Acid, Benzophenone-4, Methylisothiazolinone, Propylene Glycol, Polyquaternium-7, Sodium Citrate, Methylchloroisothiazolinone, Aloe Barbadensis Leaf Juice, Camellia Sinensia Leaf Extract, Red 33 (CI 17200), Blue 1 (CI 42090).

  • Questions?

    1-877-485-0385

  • NDC-72288-021-32

    AMAZON ESS FRESH AB 6X32OZ FHSP

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    liquid hand soap liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72288-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE130 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    POLYQUATERNIUM-7 (UNII: 0L414VCS5Y)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    BENZOPHENONE-4 (UNII: 1W6L629B4K)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    TETRASODIUM EDTA (UNII: MP1J8420LU)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72288-021-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/01/2025
    Labeler - AMAZON.COM SERVICES LLC (128990418)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(72288-021)