3M AVAGARD FOAMING INSTANT HAND ANTISEPTIC- alcohol liquid

3M Avagard Foaming Instant Hand Antiseptic by

Drug Labeling and Warnings

3M Avagard Foaming Instant Hand Antiseptic by is a Otc medication manufactured, distributed, or labeled by 3M Health Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

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

INGREDIENTS AND APPEARANCE

3M AVAGARD FOAMING INSTANT HAND ANTISEPTIC 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17518-055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	548 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Denatonium Benzoate (UNII: 4YK5Z54AT2)
PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794)
POLYETHYLENE OXIDE 1000000 (UNII: HZ58M6D839)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17518-055-02	25 in 1 CASE	05/27/2011
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 17518-055-01	12 in 1 CASE	05/27/2011
2		500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 17518-055-00	5 in 1 CASE	05/27/2011
3		1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/27/2011

Labeler - 3M Health Care (006173082)