Label: STERILLIUM MED- alcohol liquid

  • NDC Code(s): 65616-007-03, 65616-007-06, 65616-007-08
  • Packager: BODE Chemie GmbH
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • Active ingredient

    Ethyl Alcohol 85% w/w

  • Purpose

    Antiseptic

  • Uses

    • For handwashing to decrease bacteria on the skin.
    • Recommended for repeated use.
  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

  • DO NOT USE

    Do not usein or near the eyes or on mucous membranes.

    In case of contact, rinse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours
  • KEEP OUT OF REACH OF CHILDREN

    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
    • Supervise children in the use of this product
  • Inactive ingredients

    Glycerin, Isopropyl Alcohol, Myristyl Alcohol, Water.

  • PRINCIPAL DISPLAY PANEL

    BODE

    Sterillium Med

    HEALTHCARE

    PERSONNEL HAND RUB

    85% w/w ethyl alcohol with moisturizers

    Kills> 99.999% of germs in 15 seconds without water.

    Leaves hands feeling soft and healthy.

    Dermatologically Tested.

    Read Drug Facts panel before use.

    Liquid formula with

    95% natural ingredients

    Lot:

    Use by:

    Questions? Call 1-800-MEDLINE

    NDC 65615--007-06

    1000 mL 33.8 fl. oz.

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  • INGREDIENTS AND APPEARANCE
    STERILLIUM MED 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65616-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL89.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    MYRISTYL ALCOHOL (UNII: V42034O9PU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65616-007-03500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/31/201912/31/2023
    2NDC:65616-007-061000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/31/2019
    3NDC:65616-007-0850 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/31/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/31/2019
    Labeler - BODE Chemie GmbH (316039007)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company004236139manufacture(65616-007)
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