STERIZAR  ADVANCED BARRIER CONTROL- benzalkonium chloride cloth 
Unicorn Media Partners LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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STERiZAR®
Advanced Barrier Control

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 1.6 %

Purpose

Antiseptic

Use

Antibacterial Hand Wipes for Rapid Kill of Bacteria on Skin. 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

Other information

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 - 200 Wipe Bag Label

NDC 79310-305-26

STERiZAR®
Advanced Barrier Control

Antibacterial Hand Wipes

Specially formulated to kill
harmful bacteria in seconds

ALCOHOL
FREE

Kills 99.999% of germs

Ideal for killing bacteria on skin.
No need to rinse

Contents: 200 average

• HALAL MONITORING •
COMMITTEE - UK

PRINCIPAL DISPLAY PANEL - 200 Wipe Bag Label
STERIZAR   ADVANCED BARRIER CONTROL
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79310-305
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride16 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
SODIUM ETHASULFATE (UNII: 12838560LI)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79310-305-26200 in 1 BAG11/01/2020
12.35 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/01/2020
Labeler - Unicorn Media Partners LLC (117525623)

Revised: 1/2022
Document Id: 206bf653-c745-411c-9ac8-4849f4a773b6
Set id: 3798eea5-e116-48b3-8ea3-d77dfda94cca
Version: 2
Effective Time: 20220114
 
Unicorn Media Partners LLC