Hand Sanitizer Gel

Manufacturer: SHENG HE TAI INTERNATIONAL TRADING CO., LTD.
Effective date: 2020-04-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:33:31

Label at a glance#

ProductHand Sanitizer Gel

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Storage and handling

Store in cool, dry place below 104F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flames. For external use only.

OTC - WHEN USING SECTION

do not get into eyes

if contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Other information

STORAGE AND HANDLING SECTION

Store in cool, dry place below 104F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Aqua (Water), Ammonium Acryloydimethyltaurate/VP Copolymer, Eucalyptus globulus (Eucalyptus) Oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back Labels60 mL NDC: 76584-003-06

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Sanitizer Gel
ALCOHOL
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
EUCALYPTUS OIL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76584-003	76584-003-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	W59H9296ZG	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
c19e3ef1-9aa4-f856-e053-2a95a90a1454			a4638d6c-cf35-2584-e053-2995a90a6ec7	2021-05-05	Warnings	Exact identifier spl set id: a4638d6c-cf35-2584-e053-2995a90a6ec7

Reported adverse events (FAERS/openFDA)#

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