DRS CLEAN HAND

Manufacturer: THE NADREE Co., Ltd. | EQMAXON Corp.
Effective date: 2020-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:06:01

Label at a glance#

ProductDRS CLEAN HAND

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Extract, etc.

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

For the external use only

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

DOSAGE & ADMINISTRATION SECTION

Put suitable amount in your palm to cover hands and rub hands together briskly until dry.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	8807080005077	GTIN-13: 8807080005077 EAN-13: 8807080005077 GTIN storage (14 digits): 08807080005077	500ML.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74442-0004-2	2022-01-28	C162847	48780-1	d6a99b39-5515-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74442-0004-2	DRS CLEAN HAND	500 mL in 1 BOTTLE	GEL	500		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74442-0004	DRS CLEAN HAND (ALCOHOL) GEL [THE NADREE CO., LTD.]	3	Legacy NDC, 1 package rows	20200413_a2770705-a283-ece9-e053-2995a90a54df.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

DRS CLEAN HAND
Alcohol
ALOE
WATER
BUTYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74442-0004	74442-0004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE	V5VD430YW9	IACT
WATER	059QF0KO0R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	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
a326b036-9a7b-4867-e053-2a95a90af1d3			a2770705-a283-ece9-e053-2995a90a54df	2020-04-13	Warnings	Exact identifier spl id: a326b036-9a7b-4867-e053-2a95a90af1d3 spl set id: a2770705-a283-ece9-e053-2995a90a54df

Reported adverse events (FAERS/openFDA)#

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