Label: ADVANCED ALCOHOL FOAMING HAND SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 65601-802-04, 65601-802-29, 65601-802-55, 65601-802-88
  • Packager: Betco Corporation LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • ACTIVE INGREDIENT

    Ethjyl Alcohol

  • inactives

    Aloe Barbadensis Leaf Juice, D&C Green #5, PEG 10 Perfluorohexylethyl acrylate copolymer, Perluorohexylethyl alcohol, propylene glycol, water

  • dosage

    Please read entire label before using thsi product. Place enough product on your palm to tnoroughly cover your hands, Rub hands together briskyl until dry.

  • usage

    Hand sanitizer to reduce mocroorganisms on the skin.. Use this product when soap and water are not available.

  • purpose

    Antiseptic

  • keep out of reach

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

  • warnings

    For external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame.

    When using this product avoid contact with eyes. If contact occurs rinse thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs.

  • package label

    product labelpackage label

  • INGREDIENTS AND APPEARANCE
    ADVANCED ALCOHOL FOAMING HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-802
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.6787 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    HEXYL ACETATE (UNII: 7U7KU3MWT0)  
    4-CYCLOHEXYL-2-METHYL-2-BUTANOL (UNII: HFL24LW6V5)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    WATER (UNII: 059QF0KO0R) 0.2926 mL  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.25 mL  in 1 mL
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) 0.000002 mL  in 1 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.001 mL  in 1 mL
    PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N) 0.5 mL  in 1 mL
    2-(PERFLUOROHEXYL)ETHANETHIOL (UNII: 66E2ZQ1P07) 0.5 mL  in 1 mL
    TETRAHYDROLINALOOL (UNII: UM4XS5M134)  
    EBANOL (UNII: 28N247O58B)  
    2-SEC-BUTYL CYCLOHEXANONE (UNII: 5WA6R1KL5J)  
    ISOPROPYLPHENYLBUTANAL (UNII: Z92022479Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65601-802-043785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/29/2023
    2NDC:65601-802-291000 mL in 1 BAG; Type 0: Not a Combination Product12/29/2023
    3NDC:65601-802-55208175 mL in 1 DRUM; Type 0: Not a Combination Product12/29/2023
    4NDC:65601-802-88500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/29/2023
    Labeler - Betco Corporation LLC (005050158)
    Registrant - Betco Coporation LLC (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation LLC005050158manufacture(65601-802)
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