Vi Zero Doctors Sanitizer

Manufacturer
HWAJIN BIO COSMETICS CO., LTD.
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:05

Label at a glance#

ProductVi Zero Doctors Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Instant hand sanitizer to reduce bacteria on the skin.

Dosage and administration

• Spray directly on hands, covering entire surfaces of hands and fingers. • Rub hands together until dry. • Children should be supervised when using.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 66.50% v/v

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

PURPOSE

OTC - PURPOSE SECTION

Hand Sanitizer

WARNINGS

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 eyes 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

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

• Spray directly on hands, covering entire surfaces of hands and fingers.
• Rub hands together until dry.
• 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.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2371242ethanol 66.5 % Topical SprayPSN1
2371242ethanol 0.665 ML/ML Topical SpraySCD1
2371242ethanol 66.5 % Topical SpraySY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809029839019GTIN-13: 8809029839019
EAN-13: 8809029839019
GTIN storage (14 digits): 08809029839019
100 spray bottle.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78394-020-012022-01-28C16284748780-1d6a99b39-58b1-a426-e053-dadaa90af4c255f54eea-7bb2-4174-a746-d4885b5d67e6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78394-020-01Vi Zero Doctors Sanitizer100 mL in 1 BOTTLE, SPRAYSPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78394-020VI ZERO DOCTORS SANITIZER (ALCOHOL) SPRAY [HWAJIN BIO COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20200529_55f54eea-7bb2-4174-a746-d4885b5d67e6.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
78394-02078394-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
21495ce1-9782-4783-8eb8-ce6af3376dba55f54eea-7bb2-4174-a746-d4885b5d67e62020-05-29WarningsExact identifier
spl id: 21495ce1-9782-4783-8eb8-ce6af3376dba
spl set id: 55f54eea-7bb2-4174-a746-d4885b5d67e6

Reported adverse events (FAERS/openFDA)#

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