AVAGARD D- alcohol lotion 
3M ESPE Dental Products

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.

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Drug Facts

Active Ingredient

Ethyl Alcohol, 61% w/w

Purpose

Antiseptic

Uses

instant healthcare personnel hand antiseptic

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 ingredient

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

Principal Display Panel

NDC 48878-0231-7

3M ESPE

Avagard™ D

Instant Hand Antiseptic

With Moisturizers

Contains: 61% w/w ethyl alcohol

Destroys Bacteria. Not Your Skin.

Flammable, keep away from fire or flame, heat,

sparks and sources of static discharge.

REF 2317

500 ml • 16fl oz

Principal Display Panel
AVAGARD D 
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48878-0231
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48878-0231-712 in 1 CASE04/28/2011
1500 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/01/1999
Labeler - 3M ESPE Dental Products (801390852)

Revised: 11/2021
Document Id: 9a6c41a2-f87f-42b4-84e1-6509920f7330
Set id: 00c56d8d-02e6-4839-86cc-00767428d5e9
Version: 7
Effective Time: 20211115
 
3M ESPE Dental Products