UZO HAND SANITIZER- hand sanitizer liquid

UZO Hand Sanitizer by

Drug Labeling and Warnings

UZO Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ANTHOS GROUP, INC, THE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria that potentiaily 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.

Do not use

Do not use
in children less than 2 months of age
on open skin wounds

STOP USE

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

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 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.

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 15-20C(59-86F)
Avoid freezing and excessive heat about 40C(104F)

Inactive ingredients

water, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Aloe Leaf Extract

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

UZO HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79740-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYL BENZOATE (UNII: 6618K1VJ9T)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79740-005-01	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/30/2020

Labeler - ANTHOS GROUP, INC, THE (117511051)

Establishment
Name	Address	ID/FEI	Business Operations
ANTHOS GROUP, INC, THE		117511051	manufacture(79740-005)