3M AVAGARD D - alcohol lotion 
3M Health Care

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AvagardTM D
Instant Hand Antiseptic with Moisturizers

Drug Facts

Active ingredient

Ethyl Alcohol, 61% w/w

Purpose

Antiseptic

Uses

Warnings

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

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. Wet hands thoroughly with product and allow to dry.

Other information

Inactive ingredients

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

Cat. No. 9221
Made in U.S.A. for 3M Health Care,
St Paul, MN 55144-1000
(U.S.A.) 1-800-228-3957

*3MTMAvagardTM D Instant Hand Antiseptic kills greater than 99% of MRSA and greater than 98% of other harmful bacteria in 15 seconds (in vitro) while helping to maintain skin integrity. Latex glove and CHG compatible.

Patent No.
US 6,090,395;
US 6,534,069;
US 6,623,744;
US 7,081,246

Made in U.S.A. for

3M Health Care

Saint Paul, MN 55144-1000
(U.S.A.) 1-800-228-3957

34-8703-4389-3

Principal Display Panel – 88 mL Bottle Label

NDC 17518-050-01

3M AvagardTM D

Instant Hand Antiseptic with Moisturizers

Contains: 61% w/w ethyl alcohol

Destroys Bacteria.
Not Your Skin.

Effective Against MRSA*

REF 9221

88 mL 3 fl. oz.

Principal Display Panel – 88 mL Bottle Label

Principal Display Panel – 1000 mL Bottle Label

NDC 17518-050-00

3M AvagardTM D

Instant Hand Antiseptic with Moisturizers

Contains: 61% w/w ethyl alcohol

Destroys Bacteria.
Not Your Skin.

Effective Against MRSA*

Directions: Wet hands thoroughly with product and allow to dry.

Warning: Flammable

REF 9230

33.8 fl oz 1000 mL

Principal Display Panel – 1000 mL Bottle Label

3M AVAGARD D 
ethyl alcohol   lotion
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)17518-050
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol530.7 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
beheneth-10 
docosanol 
cetyl palmitate 
dimethicone 
glycerin 
polyethylene glycol 
squalane 
water 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
117518-050-0148 BOTTLE In 1 CASEcontains a BOTTLE
188 mL In 1 BOTTLEThis package is contained within the CASE (17518-050-01)
217518-050-0212 BOTTLE In 1 CASEcontains a BOTTLE
2500 mL In 1 BOTTLEThis package is contained within the CASE (17518-050-02)
317518-050-005 BOTTLE In 1 CASEcontains a BOTTLE
31000 mL In 1 BOTTLEThis package is contained within the CASE (17518-050-00)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/01/1999

Labeler - 3M Health Care (006173082)
Revised: 12/20103M Health Care