WHITE ORGANIA FRESH PURE HAND SANITIZER

Manufacturer: WHITE COSPHARM CO.,LTD.
Effective date: 2020-04-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:07:07

Label at a glance#

ProductWHITE ORGANIA FRESH PURE HAND SANITIZER

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

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
75312-0500-1	2022-01-28	C162847	48780-1	d6a99b39-6fd6-a426-e053-dadaa90af4c2	WHITE ORGANIA FRESH PURE HAND SANITIZER 500 ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75312-0500-1	WHITE ORGANIA FRESH PURE 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
75312-0500	WHITE ORGANIA FRESH PURE HAND SANITIZER (ETHANOL) GEL [WHITE COSPHARM CO.,LTD.]	1	Legacy NDC, 1 package rows	20200421_a3b7ff9d-733c-187e-e053-2995a90aefa6.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

WHITE ORGANIA FRESH PURE HAND SANITIZER
Ethanol
AMINOMETHYLPROPANOL
POLYSORBATE 20
GRAPEFRUIT
EDETATE DISODIUM
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
BUTYLENE GLYCOL
ALOE VERA LEAF
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75312-0500	75312-0500-1

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
Name	UNII	Kind
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
GRAPEFRUIT	O82C39RR8C	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
a3b7ff9d-733d-187e-e053-2995a90aefa6			a3b7ff9d-733c-187e-e053-2995a90aefa6	2020-04-17		Exact identifier spl id: a3b7ff9d-733d-187e-e053-2995a90aefa6 spl set id: a3b7ff9d-733c-187e-e053-2995a90aefa6

Reported adverse events (FAERS/openFDA)#

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