Label: BEVERLY GEL HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 10, 2024

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  • Acive Ingredient

    ethyl Alcohol

  • inactive ingredients

    Water

    Carbomer

    Dimethicone PEG-8 Laurate

    Glycerin

    EDETOL

    Fragrance

    Aloe Barbadensis Leaf Juice

  • dosage

    Place enough product on your palm to thoroughly cover your hands

    Rub hands together brisky until dry

  • indications

    Hand sanitizer to reduce microorganisms on 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 flame

    When using this product avoid contact with eyes.

    Stop use and ask doctor if irritaiton or rash occurs.

  • PRINCIPAL DISPLAY PANEL

    product label

  • INGREDIENTS AND APPEARANCE
    BEVERLY GEL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80586-801
    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
    DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18) 0.013 mL  in 1 mL
    EDETOL (UNII: Q4R969U9FR) 0.0035 mL  in 1 mL
    FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95) 0.0003 mL  in 1 mL
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) 0.0035 mL  in 1 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.00001 mL  in 1 mL
    WATER (UNII: 059QF0KO0R) 0.3 mL  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 1 mL  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80586-801-043785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/10/2024
    Labeler - Cleanslate Group LLC (117657934)
    Registrant - Betco Corportation LLC (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation LLC005050158manufacture(80586-801)
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