HANITIZER- isopropyl alcohol liquid

Hanitizer by

Drug Labeling and Warnings

Hanitizer by is a Otc medication manufactured, distributed, or labeled by Amtrust Biochemical Corp., Amtrust Biochemical Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl Alcohol 75% v/v

PURPOSE

Antiseptic

INDICATIONS & USAGE

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

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

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.

DOSAGE & ADMINISTRATION

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 SAFETY INFORMATION

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

INACTIVE INGREDIENT

glycerin, hydrogen peroxide, purified water

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANITIZER 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74132-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.75 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	0.23425 L  in 1 L
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.00125 L  in 1 L
GLYCERIN (UNII: PDC6A3C0OX)	0.0145 L  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74132-900-00	1 L in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - Amtrust Biochemical Corp. (105819316)

Establishment
Name	Address	ID/FEI	Business Operations
Amtrust Biochemical Corp		105819316	manufacture(74132-900)