Label: 5259 HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 76138-120-04
  • Packager: Innovation Specialties
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 10, 2024

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  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl alcohol 62%

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    For handwashing to decrease bacteria on the skin.

  • WARNINGS

    Warnings:Flammable, keep away from fire or flame. For external use only.

    Stop use and ask a doctor ifirritation and redness develop and persists for more than 72 hours.

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Wet hands thoroughly with product, briskly rub hands together until dry. Supervise children in the use of this product.

  • INACTIVE INGREDIENT

    Inactive ingredients:Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

  • STORAGE AND HANDLING

    Store at room temperature 15° to 30°C (59° to 86°F).

  • QUESTIONS

    Questions?Call 1-855-755 5346

    NPN# 80062390   Citrus Scent

  • SPL UNCLASSIFIED SECTION

    Made in China for Innovation Line Culver City, CA 90230

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    5259 HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76138-120
    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
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76138-120-0440 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/25/2019
    Labeler - Innovation Specialties (030837314)
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