ALCOHOL ANTISEPTIC- alcohol gel

Alcohol Antiseptic by

Drug Labeling and Warnings

Alcohol Antiseptic by is a Otc medication manufactured, distributed, or labeled by Bausch & Lomb Incorporated, Bausch Health Companies 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 this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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.

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

Inactive ingredients

glycerin, hydrogen peroxide, hydroxypropyl cellulose, purified water USP

Questions or comments?

Call: 1-800-553-5340

Marketed by:
Bausch + Lomb, a division of
Bausch Health US, LLC
Bridgewater, NJ 08807

Product of Canada

Manufactured by:
Bausch Health Companies Inc.
Laval, Quebec H7L 4A8, Canada

© 2020 Bausch & Lomb Incorporated or its affiliates

Principal Display Panel

NDC 24208-061-01

BAUSCH + LOMB

Alcohol Antiseptic 80% Topical Gel
Hand Sanitizer Non-sterile Gel

3 oz (85 g)

Not for Sale

INGREDIENTS AND APPEARANCE

ALCOHOL ANTISEPTIC 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24208-061
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24208-061-01	1 in 1 CARTON	04/13/2020
1		85 g in 1 TUBE; 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	part333A	04/13/2020

Labeler - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch Health Companies Inc.		245141858	MANUFACTURE(24208-061) , LABEL(24208-061) , PACK(24208-061)