Label: ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 71513-105-01, 71513-105-03, 71513-105-04, 71513-105-05, view more
    71513-105-06, 71513-105-50
  • Packager: Broder Bros Co.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2023

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

View All Sections
  • 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 promptly and contact Poison Control

  • Directions

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

    Store at 20° C (68° to 77°F)

  • Inactive ingredients

    Carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, water

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

    0.5 oz / 15 ml

    Dist. By: Broder Bros. Co., dba Prime Line

    Gaffney, SC 29341

  • PRINCIPAL DISPLAY PANEL

    front panel

    drug facts panel

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71513-105
    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
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71513-105-0129.57 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    2NDC:71513-105-0359.12 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202102/28/2026
    3NDC:71513-105-04236.59 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202102/28/2026
    4NDC:71513-105-05473.18 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202102/28/2026
    5NDC:71513-105-0614.79 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202102/28/2026
    6NDC:71513-105-5029.57 mL in 1 TUBE; Type 0: Not a Combination Product01/01/202102/28/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/2021
    Labeler - Broder Bros Co. (107044246)
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!