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
  • DEA Schedule: None

Drug Label Information

Updated September 24, 2024

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

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!