Label: FOAMING HAND SANITIZER- hand sanitizer liquid

  • NDC Code(s): 75044-280-16, 75044-280-31
  • Packager: American Chemical Systems II, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 24, 2024

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  • ACTIVE INGREDIENT

    Drug Facts

    Active ingredient
    Benzalkonium chloride .13%.......Antibacterial

  • PURPOSE

    Purpose
    Antibacterial

  • INDICATIONS & USAGE

    Uses

    • hand sanitizer to decrease bacteria on the skin

  • WARNINGS

    Warnings

    For external use only

    When using this product • do not get
    into eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask a doctor if
    • irritation or redness develop and condition
    persists.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions
    • wet hands thoroughly with product and
       allow to dry without wiping
    • supervise children when using this product

  • INACTIVE INGREDIENT

    Inactive ingredients Purified Water, Aloe Vera, Propylene Glycol, Triethylene Glycol, Polysorbate-20, Fragrance

  • ACS™ FOAMING HAND SANITIZER Labeling

    ACS™

    FOAMING
    HAND

    SANITIZER

    Distributed by:
    AMERICAN CHEMICAL SYSTEMS II, LLC
    2520 South Sheridan St.,
    Wichita, Kansas 67217
    (800) 889-3489

    Lot No:
    Expiry

    Labeling [2 x 1 gal. (7.6 L)]

    ACS 26116 2-per box

    1 Gal Botl

    Labeling [3-33.8 fl oz (1 L) Bottles (101.4 fl oz (3 qt 5.4 fl oz) (3 L))]

    ACS 26116 3- per Box

    ACS 26116 1000 mL Botl

    rege

  • INGREDIENTS AND APPEARANCE
    FOAMING HAND SANITIZER 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75044-280
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA FLOWER (UNII: 575DY8C1ER)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75044-280-313 in 1 CASE09/01/2024
    11000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:75044-280-162 in 1 CASE09/01/2024
    23800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/01/2024
    Labeler - American Chemical Systems II, LLC (016631058)
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