3M Avagard D: Package Insert and Label Information

3M AVAGARD D- alcohol lotion
3M Company

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 Facts

Active ingredient

Ethyl Alcohol, 61% w/w




  • 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


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.


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


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: 3M.com/patents


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
(click image for full-size original)
alcohol lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:17518-050
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (Alcohol) Alcohol 530.7 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
cetyl palmitate
Polyethylene Glycol, Unspecified
# Item Code Package Description Multilevel Packaging
1 NDC:17518-050-01 88 mL in 1 BOTTLE None
2 NDC:17518-050-02 500 mL in 1 BOTTLE None
3 NDC:17518-050-00 1000 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 10/01/1999
Labeler — 3M Company (006173082)

Revised: 06/2020 3M Company

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