3M AVAGARD FOAMING INSTANT HAND ANTISEPTIC- alcohol liquid 
3M Health Care

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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3M™ Avagard™ 
Foaming Instant Hand Antiseptic

Drug Facts

Active ingredient

Ethyl Alcohol, 70% v/v (62% w/w)

Purpose

Antiseptic

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 flame.

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 hands and fingers. Rub onto hands until dry.

  • Supervise children in the use of this product.

Other information

Store at 20-25°C (68-77°F)

Inactive Ingredients

denatonium benzoate PEG/PPG-18/18 dimethicone, PEG-23M, water

Questions?

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

Made in Canada for
3M Health Care2510 Conway Ave.St PauL MN 551443M.com/Medical

3M and Avagard are trademarks of 3M.
©2017, 3M.All rights reserved.
Patent: 3M.com/Patents
34-8720-7424-9

Principal Display Panel – 1000 mL Cartridge Label

3M NDC 17518-055-00

Avagard™ Foaming

Instant Hand Antiseptic

Contains: 70% v/v ethyl alcohol

Fragrance-Free

Latex glove and CHG compatible

Directions: Thoroughly wet hands and fingers. Rub until dry.

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

REF

9322A

33.8 fl oz • 1000 mL

Principal Display Panel – 1000 mL Cartridge Label

3M AVAGARD FOAMING INSTANT HAND ANTISEPTIC 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17518-055
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol548 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Denatonium Benzoate (UNII: 4YK5Z54AT2)  
PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794)  
POLYETHYLENE OXIDE 1000000 (UNII: HZ58M6D839)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17518-055-0225 in 1 CASE05/27/2011
150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:17518-055-0112 in 1 CASE05/27/2011
2500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3NDC:17518-055-005 in 1 CASE05/27/2011
31000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/27/2011
Labeler - 3M Health Care (006173082)

Revised: 10/2019
Document Id: d14542ab-a5b1-41ac-b8ae-e1640eb8bb00
Set id: a8c72bcf-9e60-4702-b666-72639b0505b6
Version: 11
Effective Time: 20191003
 
3M Health Care