K.vi zero Sanitizer

Manufacturer: HWAJIN BIO COSMETICS CO., LTD.
Effective date: 2020-06-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:15

Label at a glance#

ProductK.vi zero Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

Instant hand sanitizer to reduce bacteria on the skin.

Dosage and administration

• Apply product onto clean and dry hands. • Rub hands together covering all surfaces of hands and fingers until it is absorbed. • Children should be supervised when using.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHANOL 70% w/w

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Vera Gel, Mulberry Root Extract, Carbomer, Triethanolamine, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Hand Sanitizer

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.
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Do not use
• In children less than 2 months of age
• On open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Instant hand sanitizer to reduce bacteria on the skin.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply product onto clean and dry hands.
• Rub hands together covering all surfaces of hands and fingers until it is absorbed.
• Children should be supervised when using.

Other information

OTHER SAFETY INFORMATION

• Store between 1-30°C (34-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

PACKAGE LABEL : K.vi-zero Sanitizer Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tube

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

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	8809029839026	GTIN-13: 8809029839026 EAN-13: 8809029839026 GTIN storage (14 digits): 08809029839026	vi tube.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78394-030-01	2023-01-30	C162847	48780-1	f386c649-a5c9-0266-e053-dadaa90a7c1a	a10e3c7f-af6f-4efa-a780-49dce8770ac6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78394-030-01	K.vi zero Sanitizer	50 g in 1 TUBE	GEL	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78394-030	K.VI ZERO SANITIZER (ETHANOL) GEL [HWAJIN BIO COSMETICS CO., LTD.]	1	Legacy NDC, 1 package rows	20200619_a10e3c7f-af6f-4efa-a780-49dce8770ac6.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

K.vi zero Sanitizer
ETHANOL
ALCOHOL
Water
Glycerin
ALOE VERA LEAF
MORUS ALBA ROOT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78394-030	78394-030-01

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
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
Glycerin	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
MORUS ALBA ROOT	CST1G9BZGD	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	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
203e31a2-19ee-4b6c-82a4-a58b9e0a0346			a10e3c7f-af6f-4efa-a780-49dce8770ac6	2020-06-19	Warnings	Exact identifier spl id: 203e31a2-19ee-4b6c-82a4-a58b9e0a0346 spl set id: a10e3c7f-af6f-4efa-a780-49dce8770ac6

Reported adverse events (FAERS/openFDA)#

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