Nivana Hand Sanitizer Spray

Manufacturer: Dinasty Inc.
Effective date: 2020-10-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:35:25

Label at a glance#

ProductNivana Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol (Ethyl Alcohol)75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin that could potentially cause disease

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.

For external use only:hands

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age, use only under adult supervision
not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

Store below 104°F (40°C)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water USP, Glycerin, Propylene Glycol, Fragrance, Aloe Barbadensis Gel, Tocopheryl Acetate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	1
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	1
2286295	ethanol 75 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78554-007-01	2021-07-23	C162847	48780-1	c7ccaba7-205e-fd44-e053-dadaa90aa01b	Nivana Hand Sanitizer Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78554-007-01	Nivana Hand Sanitizer	60 mL in 1 BOTTLE	SPRAY	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78554-007	NIVANA HAND SANITIZER (ALCOHOL) SPRAY [DINASTY INC.]	1	Legacy NDC, 1 package rows	20201217_b17df741-13c6-c2b4-e053-2995a90a8a5d.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Nivana Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
PROPYLENE GLYCOL
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78554-007	78554-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
ALCOHOL	3K9958V90M	ACTIB

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
b17e003b-1cd7-c501-e053-2995a90a77df			b17df741-13c6-c2b4-e053-2995a90a8a5d	2020-10-12	Warnings	Exact identifier spl id: b17e003b-1cd7-c501-e053-2995a90a77df spl set id: b17df741-13c6-c2b4-e053-2995a90a8a5d

Reported adverse events (FAERS/openFDA)#

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