esthemax pharm Hand Sanitizer

Manufacturer
K Beauty Inc | GL Pharm Co., Ltd.
Effective date
2021-03-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:38:58

Label at a glance#

Productesthemax pharm Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place enough product in the palm of your hands to thoroughly cover your hands. Rub hands together briskly until product is completely absorbed and hands are dry. Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry. Inactive Ingredients:

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 83.0 %

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame. For external use only.

When using this product do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

Place enough product in the palm of your hands to thoroughly cover your hands. Rub hands together briskly until product is completely absorbed and hands are dry.

DOSAGE & ADMINISTRATION SECTION

Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Inactive Ingredients:

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredient: water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

esthemax pharm Hand Sanitizer.jpgesthemax pharm Hand Sanitizer.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74926-0010-12021-07-23C16284748780-1c7ccaba7-2751-fd44-e053-dadaa90aa01besthemax pharm hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74926-0010-1esthemax pharm Hand Sanitizer100 mL in 1 BOTTLE, PUMPGEL1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74926-0010ESTHEMAX PHARM HAND SANITIZER (ETHYL ALCOHOL) GEL [K BEAUTY INC]2Legacy NDC, 1 package rows20210313_a2d36838-d7ab-de6e-e053-2a95a90ad723.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74926-001074926-0010-1

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
GLYCERINPDC6A3C0OXIACT
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
bd5fca38-0a27-210b-e053-2a95a90a0131a2d36838-d7ab-de6e-e053-2a95a90ad7232021-03-12WarningsExact identifier
spl id: bd5fca38-0a27-210b-e053-2a95a90a0131
spl set id: a2d36838-d7ab-de6e-e053-2a95a90ad723

Reported adverse events (FAERS/openFDA)#

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