Label: ALCOHOL liquid

  • NDC Code(s): 55910-889-16, 55910-889-48
  • Packager: Old East Main Co.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 2, 2026

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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 eyues, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale of 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 plastic
  • Inactive ingredients

    water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

  • Claim

    *Effective at elimnating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

  • ADVERSE REACTION

    DISTRIBUTED BY

    OLD EAST MAIN CO,

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

    100% Satisfaction Guaranteed! (888)309-9030

  • Principal display panel

    STUDIO SELECTION ®

    moisturizing

    HAND SANITIZER with aloe

    • with Vitamin E
    • Kills 99.99% of many common germs & bacteria*

    2 FL OZ (59 mL)

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-889
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE (UNII: V5VD430YW9)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-889-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2019
    2NDC:55910-889-481005 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/201903/14/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/17/2019
    Labeler - Old East Main Co. (068331990)
    Registrant - Nice-Pak Products, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091514manufacture(55910-889)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091520manufacture(55910-889)
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