GEL HAND SANITIZER- alcohol gel

Gel Hand Sanitizer by

Drug Labeling and Warnings

Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by 74793, Streamline Polymers LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% 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

Water, Glycerin, Polyquaterniun-37, hydrogen peroxide. Fragrance

Package Label - Principal Display Panel

250 mL NDC: 74793-0005-1

500 mL NDC: 74793-0005-2 3780 mL NDC: 74793-0005-3

PRINCIPAL DISPLAY PANEL

500 mL NDC # 74793-0005-2

INGREDIENTS AND APPEARANCE

GEL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74793-0005
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
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)	0.04 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)
POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)	0.67 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74793-0005-1	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
2	NDC: 74793-0005-2	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
3	NDC: 74793-0005-3	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/06/2020

Labeler - 74793 (117054225)

Registrant - Streamline Polymers LLC (117054225)

Establishment
Name	Address	ID/FEI	Business Operations
Streamline Polymers LLC		117054225	manufacture(74793-0005)