Label: ETHYL ALCOHOL lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 24, 2022

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  • Active ingredient

    Ethyl alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For external use only: hands

    Flammable, keep away from fire or flame.

  • When using this product

    • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest
  • Stop use and ask a doctor if

    • irritation and redness develop
    • condition 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.

  • Directions

    • wet hands thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • Other information

    • do not store above 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate

  • SPL UNCLASSIFIED SECTION

    Distributed by: S.P. Richards Company, Smyrna, GA 30082
    www.genuinejoe.com

    SDS-MO-15036

    SDA-WI-2486

    DSP-MO-28

    DSP-MO-34

    447.001/447AC

  • principal display panel

    Genuine Joe

    MOISTURIZING FOAMING HAND SANITIZER

    Fragrance Free

    10453

    8 FL OZ (236 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL 
    ethyl alcohol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62832-447
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62832-447-69236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/03/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/03/2017
    Labeler - S.P. Richards Company (007976384)
    Registrant - Vi-Jon, LLC (088520668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(62832-447)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(62832-447)
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