HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Fluid USA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer.

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

• in children less than 2 months of age
• on open skin wounds

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.

STOP USE

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

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

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

237mL NDC: 76944-080-08

474mL NDC: 76944-080-16

946ml NDC: 76944-080-32

3.8L NDC: 76944-080-01

20L NDC: 76944-080-05

208L NDC: 76944-080-55

1249L NDC: 76944-080-30

24605L NDC: 76944-080-65

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76944-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76944-080-16	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
2	NDC: 76944-080-01	3785 mL in 1 JUG; Type 0: Not a Combination Product	03/30/2020
3	NDC: 76944-080-05	20000 mL in 1 PAIL; Type 0: Not a Combination Product	03/30/2020
4	NDC: 76944-080-55	208000 mL in 1 DRUM; Type 0: Not a Combination Product	03/30/2020
5	NDC: 76944-080-30	1249000 mL in 1 TANK; Type 0: Not a Combination Product	03/30/2020
6	NDC: 76944-080-65	24605000 mL in 1 TANK; Type 0: Not a Combination Product	03/30/2020
7	NDC: 76944-080-32	946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/30/2020
8	NDC: 76944-080-08	237 mL in 1 BOTTLE, SPRAY; 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 not final	part333A	03/30/2020

Labeler - Fluid USA INC (117508196)

Establishment
Name	Address	ID/FEI	Business Operations
Fluid USA INC		117508196	manufacture(76944-080)