AQUACIL- benzalkonium chloride liquid

AQUACIL by

Drug Labeling and Warnings

AQUACIL by is a Otc medication manufactured, distributed, or labeled by Inopak, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive Ingredient

Benzalkonium Chloride 0.1% W/W

Purpose

Antiseptic

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

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

Warnings

• For external use only.
• Keep out of eyes, ears or mouth. 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.

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 and rub until dry.

Inactive Ingredients

Cetrimonium chloride, laurtrimonium chloride, phenoxyethanol, stearalkonium chloride, water

PRINCIPAL DISPLAY PANEL

AQUACIL ™
INSTANT FOAMING HAND SANITIZER

KILLS 99.9% OF GERMS
Alcohol Free Formula

Benzalkonium Chloride 0.1%
For Use Without Water

biocentris PHARMACEUTICALS
888-497-4375
info@biocentrispharmaceuticals.com
www.biocentrispharmaceuticals.com

50 ml

BIO-5075-480

INGREDIENTS AND APPEARANCE

AQUACIL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58575-170
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	100 mg  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: 58575-170-02	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2013
2	NDC: 58575-170-80	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2013
3	NDC: 58575-170-18	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2013
4	NDC: 58575-170-37	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2013
5	NDC: 58575-170-10	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	05/01/2013
6	NDC: 58575-170-12	1000 mL in 1 POUCH; Type 0: Not a Combination Product	05/01/2013

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

Labeler - Inopak, Ltd (194718243)

Registrant - Inopak, Ltd (194718243)

Establishment
Name	Address	ID/FEI	Business Operations
Inopak, Ltd		194718243	manufacture(58575-170)