Label: FA HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 74932-320-01, 74932-320-02, 74932-320-03, 74932-320-04
  • Packager: HLB CO.,LTD_Healthcare
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 70% w/w

  • INACTIVE INGREDIENTS

    Carbomer, Fragrance, Glycerin, Triethanolamine, Water

  • PURPOSE

    Antiseptic

  • WARNINGS

    For external use only. Flammable. Keep away from heat or flame

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    When using this product ■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water ■ avoid contact with broken skin ■ do not inhale or ingest
    --------------------------------------------------------------------------------------------------------
    Stop use and ask a doctor if irritation or rash appears and lasts

  • KEEP OUT OF REACH OF CHILDREN

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

  • Uses

    ■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

  • Directions

    ■ Place enough product on hands to cover all surfaces. Rub hands together until dry.

    ■ Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other Information

    ■ Store below 86℉(Between 1~30℃)

    ■ May discolor certain fabrics or surfaces

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL (2mL*50pcs)

    Image of carton
    Image of carton
  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL (500mL Bottle)

    Image of bottle

    Image of bottle
  • INGREDIENTS AND APPEARANCE
    FA HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74932-320
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Glycerin (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74932-320-0250 in 1 CARTON06/01/2020
    1NDC:74932-320-012 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:74932-320-03300 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202012/30/2022
    3NDC:74932-320-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/01/2020
    Labeler - HLB CO.,LTD_Healthcare (987587913)
    Registrant - HLB CO.,LTD_Healthcare (987587913)
    Establishment
    NameAddressID/FEIBusiness Operations
    HLB CO.,LTD_Healthcare987587913manufacture(74932-320)
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