Drug Facts

Active Ingredient(s)

Benzalkonium Chloride: 1.6%

Purpose

Antiseptic

Hand Sanitizer Gel. For Hand Sanitizing to Decrease Bacteria On Skin. Safe for Repeated Use. For use when soap and water not available.

For external use only. Keep away from heat. Flammable, Keep Away from Heat and Flame

When using this product keep out of eyes 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 serious medical conditions.

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away at 1-800-222-1222

Squeeze gently approximately 2 ml (one shot) on physically clean hands.
Rub into the hands skin for at least 30 seconds ensuring that all areas are covered until dry.

Amines, C12-14 Alkyl dimethyl, Decyl Dimethyl Ammonium Chloride, N-oxides, Purified Water, Sodium Ethyl Hexyl Sulfate.

Imported and distributed by
Unicorn Media Partners LLC
41 E. Sunrise Hwy.
Lindenhurst, NY 11757

NDC 79310-303-22

STERiZAR®
Advanced Barrier Control

Bactericidal
Hand Gel
Sanitizer

Specially formulated to kill
harmful bacteria

Effective for at
least 6 hours
No need to rinse

16.9 FL OZ (500 mL)

ALCOHOL
FREE

Kills 99.999% of germs

• HALAL MONITORING •
COMMITTEE - UK

STERIZAR ADVANCED BARRIER CONTROL BACTERICIDAL HAND SANITIZER
benzalkonium chloride gel

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	16 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
SODIUM ETHASULFATE (UNII: 12838560LI)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79310-303-21	5000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
2	NDC:79310-303-22	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
3	NDC:79310-303-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
4	NDC:79310-303-27	285 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH NOT FINAL	part333A	11/01/2020

Labeler - Unicorn Media Partners LLC (117525623)