Naisture Hand Cleaner Gel(Hand Sanitizer)

Manufacturer: YOON JI CORPORATION CO.,LTD
Effective date: 2020-04-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:06:51

Label at a glance#

ProductNaisture Hand Cleaner Gel(Hand Sanitizer)

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100

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
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75024-015-10	2024-01-30	C162847	48780-1	1030e364-fbfb-111a-e063-dadaa90a10e2	Naisture Hand Sanitizer 1.5 ml x 100 : 75024-015-10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75024-015-10	Naisture Hand Cleaner Gel(Hand Sanitizer)	100 in 1 BOX	GEL	100		1
75024-015-10	Naisture Hand Cleaner Gel(Hand Sanitizer)	1.5 mL in 1 POUCH	GEL	1.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75024-015	NAISTURE HAND CLEANER GEL(HAND SANITIZER) (ETHYL ALCOHOL) GEL [YOON JI CORPORATION CO.,LTD]	1	Legacy NDC, 2 package rows	20200418_a38c8708-21b0-cea1-e053-2a95a90aae36.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Naisture Hand Cleaner Gel(Hand Sanitizer)
Ethyl Alcohol
POLYOXYL 40 HYDROGENATED CASTOR OIL
ALOE VERA LEAF
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
PANTHENOL
CHLORPHENESIN
ALCOHOL
HYDROXYETHYL CELLULOSE, UNSPECIFIED
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75024-015	75024-015-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
PANTHENOL	WV9CM0O67Z	IACT
CHLORPHENESIN	I670DAL4SZ	IACT
ALCOHOL	3K9958V90M	ACTIB
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
TROLAMINE	9O3K93S3TK	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
a38c821d-7cf3-773d-e053-2995a90aa9fa			a38c8708-21b0-cea1-e053-2a95a90aae36	2020-04-16		Exact identifier spl id: a38c821d-7cf3-773d-e053-2995a90aa9fa spl set id: a38c8708-21b0-cea1-e053-2a95a90aae36

Reported adverse events (FAERS/openFDA)#

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