Label: FAST- alcohol liquid

  • NDC Code(s): 62257-658-08, 62257-658-10, 62257-658-11, 62257-658-12, view more
    62257-658-14, 62257-658-17, 62257-658-18
  • Packager: ABC Compounding Co., Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • Drug Facts Box OTC-Active Ingredient Section

    Ethyl Alcohol 70%

  • Drug Facts Box OTC-Purpose Section

    Antiseptic

  • Drug Facts Box OTC-Indications & Usage Section

    for hand-washing to decrease bacteria on the skin, only when water is not available

  • Drug Facts Box OTC-Warnings Section

    FLAMMABLE, keep away from fire and flames

    For external use only

  • Drug Facts Box OTC-When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water

  • Drug Facts Box OTC-Stop Use Section

    irritation and redness develop

  • Drug Facts Box OTC-Keep Out of Reach of Children Section

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

  • Drug Facts Box OTC-Dosage & Administration Section

    press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand

    rub hands together and allow to dry without wiping

  • Drug Facts Box OTC-Inactive Ingredient Section

    water, peg 10 acrylate/perfluorohexylethyl acrylate copolymer, perfluorohexylethyl alcohol, propylene glycol

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  • INGREDIENTS AND APPEARANCE
    FAST 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-658
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62257-658-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2021
    2NDC:62257-658-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/06/2021
    3NDC:62257-658-111000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2021
    4NDC:62257-658-121000 mL in 1 BAG; Type 0: Not a Combination Product10/06/2021
    5NDC:62257-658-081 in 1 BOX10/06/2021
    51000 mL in 1 BAG; Type 0: Not a Combination Product
    6NDC:62257-658-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2021
    7NDC:62257-658-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/06/2021
    Labeler - ABC Compounding Co., Inc. (003284353)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(62257-658)
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