isLeaf Hand Cleaning Gel Plus

Manufacturer: C3 Co., Ltd.
Effective date: 2020-03-30
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:04:25

Label at a glance#

ProductisLeaf Hand Cleaning Gel Plus

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Astragalus Membranaceus Root Extract, Eclipta Prostrata Extract, Scutellaria Baicalensis Root Extract, Morus Alba Bark Extract, 1,2-Hexanediol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Lavandula Angustifolia (Lavender) Oil, Glycerin, Undecylenoyl Glycine, Undecylenic Acid

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Wet hands thoroughly with product

WARNINGS SECTION

For external use only.

Avoid contact with eyes.

Keep out of reach of children.

Discontinue use if skin irritation occurs.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70818-022-01	2022-01-28	C162847	48780-1	d6a99b39-6e4f-a426-e053-dadaa90af4c2	C3 Co., Ltd. - isLeaf Hand Cleaning Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70818-022-01	isLeaf Hand Cleaning Gel Plus	500 mL in 1 BOTTLE, PUMP	GEL	500		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70818-022	ISLEAF HAND CLEANING GEL PLUS (ALCOHOL) GEL [C3 CO., LTD.]	2	Legacy NDC, 1 package rows	20200331_a21d85a6-abb3-1e1c-e053-2a95a90ac040.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

isLeaf Hand Cleaning Gel Plus
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70818-022	70818-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a21d879e-1df4-21be-e053-2a95a90ae7d3			a21d85a6-abb3-1e1c-e053-2a95a90ac040	2020-03-30	Warnings	Exact identifier spl id: a21d879e-1df4-21be-e053-2a95a90ae7d3 spl set id: a21d85a6-abb3-1e1c-e053-2a95a90ac040

Reported adverse events (FAERS/openFDA)#

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