AQUACIL

Manufacturer: Inopak, Ltd
Effective date: 2019-10-30
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: legacy-cache
Hydrated at: 2026-08-02 00:04:11

Label at a glance#

ProductAQUACIL

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

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

Dosage and administration

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.

Contacts and useful links#

PhoneLabel contact888-497-4375

Websitewww.biocentrispharmaceuticals.com

www.biocentrispharmaceuticals.com

Label contents#

Full prescribing information#

Drug FactsActive Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% W/W

Purpose

OTC - PURPOSE SECTION

Antiseptic

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

OTC - STOP USE SECTION

irritation and redness develop or if condition persists for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.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

Inopak Aquacil

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BENZALKONIUM CHLORIDE	ACTIVE INGREDIENT	F5UM2KM3W7	1
BENZALKONIUM	ACTIVE MOIETY	7N6JUD5X6Y	1
1,2-HEXANEDIOL	INACTIVE INGREDIENT	TR046Y3K1G	1
CAPRYLYL GLYCOL	INACTIVE INGREDIENT	00YIU5438U	1
CETRIMONIUM CHLORIDE	INACTIVE INGREDIENT	UC9PE95IBP	1
CHLORHEXIDINE GLUCONATE	INACTIVE INGREDIENT	MOR84MUD8E	1
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	1
POLYQUATERNIUM-10 (125 MPA.S AT 2%)	INACTIVE INGREDIENT	L45WU8S981	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

AQUACIL
BENZALKONIUM CHLORIDE
BENZALKONIUM
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
PHENOXYETHANOL
STEARALKONIUM CHLORIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58575-170	58575-170-02, 58575-170-80, 58575-170-18, 58575-170-37, 58575-170-10, 58575-170-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
LAURTRIMONIUM CHLORIDE	A81MSI0FIC	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
STEARALKONIUM CHLORIDE	0OUO26BB88	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	CREAM, AUGMENTED / TOPICAL		10 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	AEROSOL, FOAM / TOPICAL		72 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	GEL / TOPICAL		14 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	CREAM / TOPICAL		57 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	AEROSOL / TOPICAL	1.05 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	LOTION / TOPICAL	1 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a0a4a0aa-e449-4c83-a78f-769175218834			ad513dd9-5c44-4c64-bb97-6ced49aae02a	2019-10-30	Warnings	Exact identifier spl id: a0a4a0aa-e449-4c83-a78f-769175218834 spl set id: ad513dd9-5c44-4c64-bb97-6ced49aae02a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.