AQUACIL- benzalkonium chloride liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Available from:

Biocentris Pharmaceuticals, LLC

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Purpose Antiseptic Uses - To help reduce bacteria on the skin that potentially can cause disease. - Recommended for repeated use.

Authorization status:

OTC monograph not final

Summary of Product characteristics

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_
To help reduce bacteria on the skin that potentially can cause
disease.
Recommended for repeated use.
_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_
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 INGREDIENTS _Cetrimonium Chloride, Laurtrimonium Chloride,
Phenoxyethanol,
Stearalkonium Chloride, Water.
Developed and Marketed by BIOCENTRIS PHARMACEUTICALS
24 Executive Parkway, Ringwood, NJ 07456
888-497-4373
[e-mail] • 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
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)
BENZ ALKONIUM
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)
Biocentris Pharmaceuticals, LLC
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM COD