FDA.reportPublic FDA data

KOBOInstant Hand Sanitizer

Manufacturer
KOBO Cosmetics Co., Ltd.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:17

Label at a glance#

ProductKOBOInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Keep away from fire or flame.

INACTIVE INGREDIENT SECTION

Water,

Caprylyl Glycol,

Glycerin, Isopropyl Myristate,

Tocopheryl Acetate,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer

Aminomethyl Propanol

Fragrance (Parfum).

INDICATIONS & USAGE SECTION

Place productin your palms and thoroughly spread on your hands. Rub hands until dry. Children must be supervised in use of this product.

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Awoid contact with broken
skin. Do not inhale or ingest.Stop use and ask a doctor if iritation or rash appears and lasts.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42001-001-012022-01-28C16284748780-1d6a99b39-3aa0-a426-e053-dadaa90af4c2a3cb2182-54d3-3643-e053-2a95a90a3806

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42001-001-01KOBOInstant Hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42001-001KOBOINSTANT HAND SANITIZER LIQUID [KOBO COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20200422_a3cb2182-54d3-3643-e053-2a95a90a3806.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42001-00142001-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
GLYCERINPDC6A3C0OXIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
a3cb2182-54d4-3643-e053-2a95a90a3806a3cb2182-54d3-3643-e053-2a95a90a38062020-04-21WarningsExact identifier
spl id: a3cb2182-54d4-3643-e053-2a95a90a3806
spl set id: a3cb2182-54d3-3643-e053-2a95a90a3806

Reported adverse events (FAERS/openFDA)#

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