FDA.reportPublic FDA data

Nivana HAND SANITIZER

Manufacturer
JINHUA KAZSHOW COSMETICS CO., LTD.
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:14

Label at a glance#

ProductNivana HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

●Store between 15-30°C(59-86°F)
●avoid feezing and excessive heat above 40°C(104°F)

INACTIVE INGREDIENT SECTION

Purified water USP, Glycerin, Propylene Glycol, Fragrance，Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

INDICATIONS & USAGE SECTION

Place enough productonhands tocover alsurfaces.Ruibhands togetherunti diry.

OTC - ACTIVE INGREDIENT SECTION

Alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54248-007-012021-07-23C16284748780-1c7ccaba7-1767-fd44-e053-dadaa90aa01ba7cbaa8a-2305-e01f-e053-2995a90a6be4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54248-007-01Nivana HAND SANITIZER60 mL in 1 BOTTLESPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54248-007NIVANA HAND SANITIZER (ALCOHOL) SPRAY [JINHUA KAZSHOW COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20200611_a7cbaa8a-2305-e01f-e053-2995a90a6be4.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54248-00754248-007-01

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
ALOEV5VD430YW9IACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
GLYCERINPDC6A3C0OXIACT

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
a7cbaa8a-2306-e01f-e053-2995a90a6be4a7cbaa8a-2305-e01f-e053-2995a90a6be42020-06-11WarningsExact identifier
spl id: a7cbaa8a-2306-e01f-e053-2995a90a6be4
spl set id: a7cbaa8a-2305-e01f-e053-2995a90a6be4

Reported adverse events (FAERS/openFDA)#

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