BIOCENTRIS E2 HANDWASH- benzalkonium chloride liquid 
Biocentris Pharmaceuticals, 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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Biocentris E2 Foam Handwash

Drug Facts

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

Antiseptic

Uses

Warnings

For external use only.

When using this product keep away from eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

Directions

Inactive ingredients Water, Ethanol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Phenoxyethanol, Polyquatemium 11, Decyl Glucoside, Cetrimonium Chloride, Polyquatemium-10, Chlorhexidine Gluconate

Manufactured for:

biocentris PHARMACEUTICALS

24 Executive Parkway, Ringwood, NJ 07456

888-497-4375

info@biocentris.com • www.biocentris.com

E2 FOAM HANDWASH FOR FOOD INDUSTRY PROFESSIONALS

One Step Hand Wash & Sanitizer

KILLS 99.99% of most germs

NET CONTENTS: 33.8 FL. OZ. (1000 ML)

81232-402 BioCentris E2-0622

BIOCENTRIS E2 HANDWASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81232-402
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
ALCOHOL (UNII: 3K9958V90M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)  
POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81232-402-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
2NDC:81232-402-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
3NDC:81232-402-011000 mL in 1 POUCH; Type 0: Not a Combination Product04/20/2021
4NDC:81232-402-17532 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2018
Labeler - Biocentris Pharmaceuticals, LLC (015882747)

Revised: 6/2022
Document Id: e2ae1bbb-5f12-e5d4-e053-2995a90a4180
Set id: b61f97d8-8c33-0a9f-e053-2a95a90a5531
Version: 3
Effective Time: 20220630
 
Biocentris Pharmaceuticals, LLC