ALCOHOL FREE HAND SANITIZER- benzalkonium chloride solution

Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Hybrisan Ltd, Gwalia Healthcare Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Benzalkonium Chloride 0.13% Purpose Antiseptic

Drug Facts

Antiseptic

Drug Facts

For personal hand sanitizing and to reduce bacteria on the skin. Recommended for repeated use

Avoid contact with eyes. In the case of eye contact flush eyes with water.

Warnings

When using this product avoid contact with eyes. In case of eye contact flush eyes with water.

Ask Doctor

Stop use and ask a doctor if irritation and redness develop

Inactive ingredients

Fragrances, water

Directions

Apply liberally to the hands and gently rub until dry

Questions?

Telephone: 44-1639-898150 Monday through Friday 8:00am til 4:30pm UK time

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.

Package quantity

100ml (3.38 Floz) NDC: 81685-321-10

INGREDIENTS AND APPEARANCE

ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81685-321
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
3A,4,5,6,7,7A-HEXAHYDRO-1H-4,7-METHANOINDEN-6-YL ACETATE (UNII: 5232EN3X2F)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
.ALPHA.-TERPINEOL (UNII: 21334LVV8W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
METHYL HEPTINE CARBONATE (UNII: 0TTP6YT2T3)

Product Characteristics
Color	yellow (Clear liquid)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81685-321-10	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2021

Labeler - Hybrisan Ltd (219599200)

Establishment
Name	Address	ID/FEI	Business Operations
Hybrisan Ltd		219599200	manufacture(81685-321)

Establishment
Name	Address	ID/FEI	Business Operations
Gwalia Healthcare Limited		220632253	pack(81685-321)