KAZU Hand Sanitizer

Manufacturer: N Bridge Inc. | K.Boeun Pharmaceutical Co.,Ltd.
Effective date: 2020-05-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:58

Label at a glance#

ProductKAZU Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Tromethamine, Green Tea Extract, Aloe Extract

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 and allow to dry without wiping

for children under 6, use only under adult supervision

not recommended for infants

WARNINGS SECTION

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

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76966-0002-1	2022-07-29	C162847	48780-1	e4f33bdf-ac7f-d8a0-e053-dadaa90a6e4e	a611ee21-d63c-8204-e053-2a95a90a0e55

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76966-0002-1	KAZU Hand Sanitizer	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76966-0002	KAZU HAND SANITIZER (ALCOHOL) GEL [N BRIDGE INC.]	1	Legacy NDC, 1 package rows	20200521_a611ee21-d63c-8204-e053-2a95a90a0e55.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

KAZU Hand Sanitizer
ALCOHOL
ALOE
WATER
TROLAMINE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
GREEN TEA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76966-0002	76966-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE	V5VD430YW9	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
GREEN TEA LEAF	W2ZU1RY8B0	IACT

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
a611902e-553a-a578-e053-2995a90a8b6e			a611ee21-d63c-8204-e053-2a95a90a0e55	2020-05-20	Warnings	Exact identifier spl id: a611902e-553a-a578-e053-2995a90a8b6e spl set id: a611ee21-d63c-8204-e053-2a95a90a0e55

Reported adverse events (FAERS/openFDA)#

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