ALCOHOL ANTISEPTIC- alcohol solution

Alcohol Antiseptic by

Drug Labeling and Warnings

Alcohol Antiseptic by is a Otc medication manufactured, distributed, or labeled by Bausch & Lomb Incorporated, Shandong Bausch & Lomb Freda Pharm. Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 80% v/v

Purpose

Antiseptic

Uses

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, purified water USP

Questions?

Call: 1-800-553-5340

Bausch + Lomb, a division of Bausch Health US, LLC, Bridgewater, NJ 08807 USA

© 2020 Bausch & Lomb Incorporated or its affiliates

Product of China

3846300

Package/Label Principal Display Panel – Label back

Package/Label Principal Display Panel Label front -Label back

NDC 24208-060-02

BAUSCH + LOMB

Alcohol
Antiseptic 80%
Solution

Hand Sanitizer
Non-sterile Solution

Not for Sale

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

ALCOHOL ANTISEPTIC 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24208-060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 g  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: 24208-060-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2020

Labeler - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong Bausch & Lomb Freda Pharm. Co., Ltd		654512375	MANUFACTURE(24208-060) , LABEL(24208-060) , PACK(24208-060)