Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 1.6 %

Purpose

Antiseptic

Use(s)

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

Warnings

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

Do not use

On open skin wounds

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 rush occurs These may be sign 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

Directions

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

Other information

Store in cool dry area.
Avoid freezing
Store at 15-30 C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

NDC 79310-304-23

STERiZAR®
Advanced Barrier Control

Hand Foam
Sanitizer

Specially formulated to kill
harmful bacteria in seconds

ALCOHOL
FREE

Kills 99.999% of germs

Remains effective after application for at
least 6 hours using Advanced Barrier Control.
No need to rinse. Moisturizing foam that
is kind to your hands.

3.4 FL OZ (100 mL)

• HALAL MONITORING •
COMMITTEE - UK

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

STERIZAR ADVANCED BARRIER CONTROL
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79310-304
Route of Administration	TOPICAL

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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79310-304-25	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
2	NDC:79310-304-23	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
3	NDC:79310-304-22	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
4	NDC:79310-304-21	5000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020

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)

STERiZAR® Advanced Barrier Control