Label: 3M AVAGARD D- alcohol lotion

  • NDC Code(s): 17518-050-00, 17518-050-01, 17518-050-02
  • Packager: 3M Company
  • 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 June 30, 2020

If you are a consumer or patient please visit this version.


    Drug Facts

  • Active ingredient

    Ethyl Alcohol, 61% w/w

  • Purpose


  • Uses

    • instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease
    • instant hand antiseptic to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

    For external use only. Flammable, keep away from fire or flames.

    When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

    Stop use and ask a doctor if significant irritation or sensitization develops.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hand and fingers. Rub on to hands until dry.

    • Supervise children in the use of this product.
  • Other information

    • Store at 20-25°C (68-77°F)
  • Inactive ingredients

    beheneth-10, behenyl alcohol, C20-40 pareth-24, cetyl palmitate, diisopropyl dimer dilinoleate, dimethicone, glycerin, polyethylene glycol, squalane, water

  • Questions?

    call 1-800-228-3957 (Monday to Friday 7AM-6PM CST)

    Made in U.S.A. of globally sourced materials for

    3M Health Care, 2510 Conway Ave., St. Paul, MN 55144

    3M and Avagard are trademarks of 3M.

    © 2017, 3M. All rights reserved. Patent:


  • Principle Display Panel – 1000 mL Bottle Label

    NDC 17518-050-00


    Avagard™ D

    Instant Hand Antiseptic with Moisturizer

    Contains: 61% w/w ethyl alcohol

    Destroys Bacteria. Not Your Skin.

    Directions: Apply sufficient amount to thoroughly wet hands and fingers.

    Rub until dry.

    Flammable, keep away from fire or flame, heat, sparks and sources of static discharge

    REF 9230

    33.8 fl oz • 1000 mL

    Principle Display Panel – 1000 mL Bottle Label
    alcohol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17518-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol530.7 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Beheneth-10 (UNII: 313S43DM16)  
    docosanol (UNII: 9G1OE216XY)  
    cetyl palmitate (UNII: 5ZA2S6B08X)  
    dimethicone (UNII: 92RU3N3Y1O)  
    glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    squalane (UNII: GW89575KF9)  
    water (UNII: 059QF0KO0R)  
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17518-050-0188 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/1999
    2NDC:17518-050-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/1999
    3NDC:17518-050-001000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/1999
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/01/1999
    Labeler - 3M Company (006173082)