STERIZAR ADVANCED BARRIER CONTROL- benzalkonium chloride soap

STERiZAR by

Drug Labeling and Warnings

STERiZAR by is a Otc medication manufactured, distributed, or labeled by Unicorn Media Partners LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 1.6 %

Purpose

Antiseptic

Use

Sanitizing Hand Wash for Hand Washing to Decrease Bacteria on Skin. For Repeated Use.

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

• Apply a small amount of product to the hands and rub in well, paying particular attention to fingernails and the area between the fingers.
• Allow hands to air dry.
• Important- the use of towels or tissue may lead to recontamination with bacteria.

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

NDC: 79310-302-22

STERiZAR®
Advanced Barrier Control

Antibacterial
Sanitizing
Hand Wash

Specially formulated to kill
harmful bacteria

ALCOHOL
FREE
Kills 99.999% of germs

2 Hours
Protection after Rinsing

16.9 FL OZ (500 mL)

HALAL MONITORING
COMMITTEE - UK

INGREDIENTS AND APPEARANCE

STERIZAR   ADVANCED BARRIER CONTROL
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79310-302
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79310-302-22	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2020
2	NDC: 79310-302-21	5000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/01/2020
3	NDC: 79310-302-27	285 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/01/2020

Labeler - Unicorn Media Partners LLC (117525623)