AQUACIL- 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.

----------

Biocentris Aquacil

Drug Facts

Active ingredient

Benzalkonium chloride 0.1% (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 or redness develop or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients Cetrimonium Chloride, Laurtrimonium Chloride, Phenoxyethanol, Stearalkonium Chloride, Water.

Developed and Marketed by biocentris PHARMACEUTICALS

24 Executive Parkway, Ringwood, NJ 07456

888-497-4373

info@biocentris.com • www.biocentris.com

AQUACIL®
FOAMING HAND SANITIZER

Benzalkonium Chloride 0.1%

KILLS 99.9% OF GERMS
Alcohol Free Formula

33.8 fl oz (1000 mL)

Aquacil Instant Foaming HS_BZK

AQUACIL 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81232-170
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81232-170-0350 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2013
2NDC:81232-170-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/201306/07/2021
3NDC:81232-170-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/201306/07/2021
4NDC:81232-170-373785 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/201306/07/2021
5NDC:81232-170-431000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product05/01/2013
6NDC:81232-170-101000 mL in 1 POUCH; Type 0: Not a Combination Product05/01/2013
7NDC:81232-170-17532 mL in 1 BOTTLE; Type 0: Not a Combination Product06/07/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2013
Labeler - Biocentris Pharmaceuticals, LLC (015882747)

Revised: 6/2021
Document Id: c42ed664-8bf1-a37a-e053-2995a90af4fa
Set id: b61f0174-528e-2b23-e053-2995a90ac9e6
Version: 2
Effective Time: 20210607
 
Biocentris Pharmaceuticals, LLC