NOVAGEL ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride hand sanitizer liquid

NovaGel Alcohol-free Foaming Hand Sanitizer by

Drug Labeling and Warnings

NovaGel Alcohol-free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Hongshiliang Health Technology Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Principle Display Panel

Active Ingredient

Active Ingredient Purpose

Benzalkonium chloride 0.1% Antimicrobial

Use

To decrease bacteria on skin

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.

Warning

Warnings. For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stope use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

Directions - Pump a small amount of foam onto palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Inactive ingredients

Inactive ingredients- water, glycerin, sodium lauryl sulfate, fragrance

Dosage and Adminstration Section

Benzalkonium Chloride 0.1%

Directions - Pump a small amount of foam onto palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Purpose Section

Purpose

Antimicrobial

INGREDIENTS AND APPEARANCE

NOVAGEL ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78360-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	97.1 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	2 g  in 100 g
SODIUM LAURYL SULFATE (UNII: 368GB5141J)	0.5 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78360-001-01	59.15 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/26/2020

Labeler - Zhejiang Hongshiliang Health Technology Co Ltd (553365550)