Nature Hand Touch Antiseptic Ethanol

Manufacturer: Dai Kyoung Pharmaceutic Co.,Ltd.
Effective date: 2020-04-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:05:03

Label at a glance#

ProductNature Hand Touch Antiseptic Ethanol

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

water, glycerin, triethanolamine, etc

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS SECTION

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

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labell

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2287156	ethanol 83 % Topical Solution	PSN	2
2287156	ethanol 0.83 ML/ML Topical Solution	SCD	2
2287156	ethyl alcohol 83 % Topical Solution	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74279-0004-1	2022-07-29	C162847	48780-1	e4f33bdf-a306-d8a0-e053-dadaa90a6e4e	PLUS / Dai Kyoung Pharmaceutic Co.,Ltd. - Nature Hand Touch Antiseptic Ethanol
74279-0004-2	2022-07-29	C162847	48780-1	e4f33bdf-a306-d8a0-e053-dadaa90a6e4e	PLUS / Dai Kyoung Pharmaceutic Co.,Ltd. - Nature Hand Touch Antiseptic Ethanol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74279-0004-1	Nature Hand Touch Antiseptic Ethanol	500 mL in 1 BOTTLE, PUMP	LIQUID	500		2
74279-0004-2	Nature Hand Touch Antiseptic Ethanol	100 mL in 1 BOTTLE, SPRAY	LIQUID	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74279-0004	NATURE HAND TOUCH ANTISEPTIC ETHANOL (ALCOHOL) LIQUID [DAI KYOUNG PHARMACEUTIC CO.,LTD.]	2	Legacy NDC, 2 package rows	20200406_00da35b2-5946-4c1b-991c-9b2d88d22acf.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Nature Hand Touch Antiseptic Ethanol
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74279-0004	74279-0004-1, 74279-0004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	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
a29bd60e-de50-4695-e053-2995a90aa216			00da35b2-5946-4c1b-991c-9b2d88d22acf	2020-04-06	Warnings	Exact identifier spl id: a29bd60e-de50-4695-e053-2995a90aa216 spl set id: 00da35b2-5946-4c1b-991c-9b2d88d22acf

Reported adverse events (FAERS/openFDA)#

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