Hand Sanitizer

Manufacturer: SHENG HE TAI INTERNATIONAL TRADING CO., LTD.
Effective date: 2020-05-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:32:23

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store in a 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 and flames. For external use only

OTC - WHEN USING SECTION

When using this product 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 and redness develop.

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

STORAGE AND HANDLING SECTION

Store in a cool, dry place below 104F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), Ammonium Acryloyldimethylteurate/VP Copolymer, Eucalyptus globulus (Eucalyptus) Oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display Panel and Drug Facts100 mL NDC: 76584-005-10

Products#

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

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

Hand Sanitizer
ALCOHOL
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
EUCALYPTUS OIL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76584-005	76584-005-10

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
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

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
c29f7129-aa9d-09e0-e053-2a95a90acd40			a517dfe5-e49b-5f2d-e053-2a95a90a2ec1	2021-05-18	Warnings	Exact identifier spl set id: a517dfe5-e49b-5f2d-e053-2a95a90a2ec1

Reported adverse events (FAERS/openFDA)#

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