Hestia Clinic Gel Hand Sanitizer

Manufacturer
DongbangCosmetics Co., ltd.
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:06:04

Label at a glance#

ProductHestia Clinic Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Butylene Glycol, etc.

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Store under 30°C (86°F)

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

DOSAGE & ADMINISTRATION SECTION

Take an appropriate amount of hand sanitizing gel on your hand.

Rub your palms.

Clasp and rub it between your fingers.

Once again, take an appropriate amount of the gel on your hand.

Rub the fingernails of both hands.

Cover your finger with your palm and rub it.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2121

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74002-0100-12022-01-28C16284748780-1d6a99b39-891e-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74002-0100-1Hestia Clinic Gel Hand Sanitizer100 mL in 1 TUBEGEL1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74002-0100HESTIA CLINIC GEL HAND SANITIZER (ALCOHOL) GEL [DONGBANGCOSMETICS CO., LTD.]2Legacy NDC, 1 package rows20200413_a325c32e-da29-674a-e053-2995a90a5956.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74002-010074002-0100-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a325c32e-da2c-674a-e053-2995a90a5956a325c32e-da29-674a-e053-2995a90a59562020-04-13WarningsExact identifier
spl id: a325c32e-da2c-674a-e053-2995a90a5956
spl set id: a325c32e-da29-674a-e053-2995a90a5956

Reported adverse events (FAERS/openFDA)#

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