Label: ANTIBACTERIAL HAND SANITIZER- ethyl alcohol spray

  • NDC Code(s): 71513-202-30, 71513-202-31
  • Packager: Broder Bros Co.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2025

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

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    For hand sanitizing

  • Warnings

    • Flammable.Keep away from heat and flame.
    • For external use only.

    When using this product

    • Keep out of eyes
    • In case of contact with eyes, flush thoroughly with water
    • Avoid contact with broken skin
    • Do not inhale or ingest

    Stop use and ask a doctor

    if irritation and redness develops and persists for more than 72 hours

    Keep out of reach of children

    If swallowed get medical help or call a Poison Control Center right away

  • Directions

    • Wet hands thoroughly with product, briskly rub together until dry.
    • Always supervise children in use of this product.
    • Children under 6 months of age: Ask a doctor.
  • Other information

    Store at 66° to 77° F (22° to 25° C)

  • Inactive ingredients

    Aloe Barbadensis Leaf Extract, Carbomer, Deionizer Water, Fragrance, Glycerin, Propylene Glycol, Tocopherol Acetate, Triethanolamine

  • Questions?

    1-800-873-7746 M-F 8 am - 5 pm EST

  • SPL UNCLASSIFIED SECTION

    Net wt. 10 mL/0.33 fl. oz.

    Made in China

    Dist. By Broder Bros Co., dba Prime Line

    Gaffney, SC 29341

  • PRINCIPAL DISPLAY PANEL

    label

    drug facts

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71513-202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71513-202-3010 mL in 1 BOTTLE; Type 0: Not a Combination Product11/17/2025
    2NDC:71513-202-3120 mL in 1 BOTTLE; Type 0: Not a Combination Product11/17/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/17/2025
    Labeler - Broder Bros Co. (107044246)