Label: HAND SANITIZER- alcohol liquid

  • NDC Code(s): 53329-209-12, 53329-209-37, 53329-209-74, 53329-209-80, view more
    53329-209-98
  • Packager: Medline Industries, LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 29, 2024

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  • Active ingredient

    Ethyl alcohol 70% v/v

  • Purpose

    Antiseptic

  • Use

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

    For external use only: hands only

    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 or redness develops
    • condition persists for more than 72 hours

    Keep out of reach 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 suervision
    • not recommended for infants
  • Other information

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

    glycerin, glyceryl caprylate/caprate, isopropyl myristate, meadowfoamamidopropyl betaine, PEG-8 dimethicone, tocopheryl acetate, water

  • Manufacturing Information

    Manufactured for:

    Medline Industries, LP

    Three Lakes Drive, Northfield, IL 60093 USA

    Made in USA with US and foreign components

    www.medline.com

    1-800-MEDLINE

    REF: HH701200F

    V2 RB23VJO

  • Package Label

    Front Label V2 RB23VJO

    Back Label V2 RB23VJO

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-209
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.879 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-209-981000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/27/2016
    2NDC:53329-209-80532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/27/2016
    3NDC:53329-209-37221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/27/2016
    4NDC:53329-209-741200 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
    5NDC:53329-209-1244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/27/2016
    Labeler - Medline Industries, LP (025460908)
    Registrant - Medline Industries, LP (025460908)
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