NATURIA HAND SANITIZER

Manufacturer: WHAIN COSMETIC
Effective date: 2020-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:06:15

Label at a glance#

ProductNATURIA HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Uses: Disinfection of hands and skin

Dosage and administration

Directions: Take an appropriate amount on your hands and rub thoroughly to dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ALCOHOL 70.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water,Glycerin,Carbomer,Aminomethyl Propanol,Sodium Hyaluronate,Butylene Glycol,Camellia Sinensis Leaf Extract,Artemisia Princeps Extract

Purpose

OTC - PURPOSE SECTION

Purpose: SANITIZER

Warnings

WARNINGS SECTION

Warnings:

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

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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Uses:

Disinfection of hands and skin

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

Take an appropriate amount on your hands and rub thoroughly to dry.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73823-020-01	2023-01-30	C162847	48780-1	f386c64a-0537-0266-e053-dadaa90a7c1a	c6f98b66-f196-41a5-a3ea-43c6b6336972

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73823-020-01	NATURIA HAND SANITIZER	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73823-020	NATURIA HAND SANITIZER (ALCOHOL) GEL [WHAIN COSMETIC]	1	Legacy NDC, 1 package rows	20200414_c6f98b66-f196-41a5-a3ea-43c6b6336972.zip

Products#

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

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

NATURIA HAND SANITIZER
ALCOHOL
Water
Glycerin
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
AMINOMETHYLPROPANOL
HYALURONATE SODIUM
Butylene Glycol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73823-020	73823-020-01

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
Glycerin	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
Butylene Glycol	3XUS85K0RA	IACT

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
992ba3d4-a787-4895-9c72-f86ce1232853			c6f98b66-f196-41a5-a3ea-43c6b6336972	2020-04-13	Warnings	Exact identifier spl id: 992ba3d4-a787-4895-9c72-f86ce1232853 spl set id: c6f98b66-f196-41a5-a3ea-43c6b6336972

Reported adverse events (FAERS/openFDA)#

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