FDA.reportPublic FDA data

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

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

Primary Display and Drug Facts LabelPrimary Display and Drug Facts Label80 mL NDC: 76584-005-08

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76584-00576584-005-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS OIL2R04ONI662IACT
CARBOMER 1342809Y72KV36IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c29f7cd1-2e58-78ec-e053-2995a90a6b6ca515ee56-4127-24ce-e053-2995a90a305f2021-05-18WarningsExact identifier
spl set id: a515ee56-4127-24ce-e053-2995a90a305f

Reported adverse events (FAERS/openFDA)#

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