AQUACIL- benzalkonium chloride liquid

AQUACIL by

Drug Labeling and Warnings

AQUACIL by is a Otc medication manufactured, distributed, or labeled by Biocentris Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.1% (w/w)

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

• To help reduce bacteria on the skin that potentially can cause disease.
• Recommended for repeated use.

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

• Pump sufficient amount of foam into palm of hand.
• Wet all surfaces of both hands thoroughly with product, including the area under the fingernails.
• Rub hands together until dry.

INACTIVE INGREDIENT

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

SPL UNCLASSIFIED SECTION

Developed and Marketed by biocentris PHARMACEUTICALS

24 Executive Parkway, Ringwood, NJ 07456

888-497-4373

info@biocentris.com www.biocentris.com

PRINCIPAL DISPLAY PANEL

AQUACIL®
FOAMING HAND SANITIZER

Benzalkonium Chloride 0.1%

KILLS 99.9% OF GERMS
Alcohol Free Formula

33.8 fl oz (1000 mL)

INGREDIENTS AND APPEARANCE

AQUACIL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81232-170
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81232-170-03	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2013
2	NDC: 81232-170-08	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2013	06/07/2021
3	NDC: 81232-170-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2013	06/07/2021
4	NDC: 81232-170-37	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2013	06/07/2021
5	NDC: 81232-170-43	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	05/01/2013
6	NDC: 81232-170-10	1000 mL in 1 POUCH; Type 0: Not a Combination Product	05/01/2013
7	NDC: 81232-170-17	532 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2013

Labeler - Biocentris Pharmaceuticals, LLC (015882747)