FDA.reportPublic FDA data

V zero Hand Clean Gel

Manufacturer
KONAD CO LTD
Effective date
2022-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:53

Label at a glance#

ProductV zero Hand Clean Gel
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

3) Storage and cautions for handling. b) Avoid storing under direct sunlight, hot and cool place.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Triethanolamine, Carbomer, Glycerin, Aloe Barbadensis Leaf Extract, Sophora Flavescens Root Extract, Camellia Sinensis Leaf Extract, 1,2-Hexanediol, Phenoxyethanol, Fragrance, Ethylhexylglycerin

Hand Clean Gel

DOSAGE & ADMINISTRATION SECTION

A hand cleaner that is esay to carry and can use without water directly.

HOW TO USE

INDICATIONS & USAGE SECTION

1. Pump the appropriate amount on your palm.

2. Rub palm, back of hand, wrist, between fingers and under nail for 15 seconds.

3. Rub and dry.

CAUTIONS IN USE

OTC - DO NOT USE SECTION

2) Do not apply it on skin where you have eczema, wounded, irritated.

CAUTIONS IN USE

OTC - ASK DOCTOR SECTION

1) If anyone of following symptoms such as red spot, swollenness and/or itching, occurs when using cosmetics, or symptoms appear by direct sunlight. Stop using it and consult a doctor immediately.

CAUTIONS IN USE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

a) Keep out of the reach of children.

CAUTIONS IN USE

STORAGE AND HANDLING SECTION

3) Storage and cautions for handling. b) Avoid storing under direct sunlight, hot and cool place.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50ml NDC: 74740-598-01 Package50ml NDC: 74740-598-01 Package

50ml NDC: 74740-598-02 Outer Package Label50ml NDC: 74740-598-02 Outer Package Label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74740-59874740-598-01, 74740-598-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
1,2-HEXANEDIOLTR046Y3K1GIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT

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
0406c181-f28f-3485-e063-6394a90a2ef1a28e8e4c-5248-7dd6-e053-2a95a90a84832023-08-28WarningsExact identifier
spl set id: a28e8e4c-5248-7dd6-e053-2a95a90a8483

Reported adverse events (FAERS/openFDA)#

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