Zoosh Antiseptic Hand Sanitizer Gel, 80% Ethyl Alcohol

Manufacturer: CHESSER CHEMICALS PTY. LTD.
Effective date: 2022-09-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:53:49

Label at a glance#

ProductZoosh Antiseptic Hand Sanitizer Gel, 80% Ethyl Alcohol

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammaable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in the eyes

Stop use and ask a doctor

OTC - STOP USE SECTION

irritation and redness develops
condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Other information:

SPL UNCLASSIFIED SECTION

Store between 59-86ºF (215-30ºC)
Avoid freezing and excessive heat above 104ºF(40ºC)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, glycerin, carbomer, hydrogen peroxide, aminopropanol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Zoosh Antiseptic Hand Sanitizer Gel, 80% Ethyl Alcohol
ALCOHOL
AMINOMETHYLPROPANOL
WATER
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
HYDROGEN PEROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90088-000	90088-000-05

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
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

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
e894e943-3fbc-0eb9-e053-2995a90aa5c8			acc48024-a904-28ab-e053-2a95a90a3c01	2022-09-13	Warnings	Exact identifier spl id: e894e943-3fbc-0eb9-e053-2995a90aa5c8 spl set id: acc48024-a904-28ab-e053-2a95a90a3c01

Reported adverse events (FAERS/openFDA)#

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