ALCOHOL - HAND SANITIZER- alcohol solution

Alcohol - Hand Sanitizer by

Drug Labeling and Warnings

Alcohol - Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by AbbVie Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient[s]

Alcohol 80% v/v

Purpose

Antiseptic

Use[s]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

QUESTIONS

Questions? Tel: 1-800-633-9110

Manufactured by: AbbVie Inc. North Chicago, IL 60064

PRINCIPAL DISPLAY PANEL

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

300 mL

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

1000 mL

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

2000 mL

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

20 L

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

200 L

INGREDIENTS AND APPEARANCE

ALCOHOL - HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0074-9857
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0074-9857-05	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/25/2020
2	NDC: 0074-9857-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/25/2020
3	NDC: 0074-9857-15	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/25/2020
4	NDC: 0074-9857-20	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/25/2020
5	NDC: 0074-9857-25	200000 mL in 1 DRUM; Type 0: Not a Combination Product	03/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/25/2020

Labeler - AbbVie Inc. (078458370)