LIFEBUOY HAND SANITIZER 75 PERCENT- alcohol gel

Lifebuoy Hand Sanitizer by

Drug Labeling and Warnings

Lifebuoy Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by UNILEVER ASIA PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 75% v/v

PURPOSE

ANTISEPTIC

USE

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

• On 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, 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.

INACTIVE INGREDIENTS

Purified Water USP, Carbomer, Propylene Glycol, Aminomethyl Propanol, PEG-12 Dimethicone, Disodium EDTA, Aloe Barbadensis Extract, Maltodextrin, Potassium Sorbate, Sodium Benzoate

OTHER INFORMATION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIFEBUOY HAND SANITIZER  75 PERCENT
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50069-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50069-104-11	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/19/2020

Labeler - UNILEVER ASIA PRIVATE LIMITED (894632699)