INSTANT HAND SANITIZER

Manufacturer
Hangzhou KEON Biotech Co., Ltd.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:13

Label at a glance#

ProductINSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Directions wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Other information store below 1os °F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 67.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Use for hand-washing to decrease bacteria on the skin, only when wafer is not available.

Warnings

WARNINGS SECTION

Warnings Flammable, keep away from fire and flame. For external use only.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

When using this product Do not get into eyes.
If contact occurs, rinse eyes thoroughly witti water. May discolor some fabrics.

OTC - STOP USE SECTION

Stop use and ask a doctor if Irritation and redness develop.

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

Directions wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Other information store below 1os °F

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, GLYCERIN, CARBOMER, TRIETHANOLAMINE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79744-001-01 3780mL79744-001-01 3780mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039708ethanol 67 % Topical GelPSN1
1039708ethanol 0.67 ML/ML Topical GelSCD1
1039708ethanol 67 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79744-001-012022-01-28C16284748780-1d6a99b39-78eb-a426-e053-dadaa90af4c279744-001 INSTANT HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79744-001-01INSTANT HAND SANITIZER3780 mL in 1 BOTTLEGEL37801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79744-001INSTANT HAND SANITIZER GEL [HANGZHOU KEON BIOTECH CO., LTD.]1Legacy NDC, 1 package rows20200820_ad3589aa-c21f-49e0-e053-2a95a90adb60.zip

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
79744-00179744-001-01

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ad3589aa-c211-49e0-e053-2a95a90adb60ad3589aa-c21f-49e0-e053-2a95a90adb602020-08-19WarningsExact identifier
spl id: ad3589aa-c211-49e0-e053-2a95a90adb60
spl set id: ad3589aa-c21f-49e0-e053-2a95a90adb60

Reported adverse events (FAERS/openFDA)#

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