MAMU Hand Sanitizer gel

Manufacturer: Cnt Dream. Co., Ltd
Effective date: 2020-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:05:46

Label at a glance#

ProductMAMU Hand Sanitizer gel

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

water, etc

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.

Supervise children in the use of this product.

WARNINGS SECTION

For external use only.

Flammable.

Keep away from fire or flame.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2282911	ethanol 71 % Topical Gel	PSN	1
2282911	ethanol 0.71 ML/ML Topical Gel	SCD	1
2282911	ethanol 71 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71909-0001-1	2022-01-28	C162847	48780-1	d6a99b39-d65c-a426-e053-dadaa90af4c2	CNT DREAM (AMARTE) - MAMU Hand Sanitizer gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71909-0001-1	MAMU Hand Sanitizer gel	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
71909-0001	MAMU HAND SANITIZER GEL (ALCOHOL) GEL [CNT DREAM. CO., LTD]	1	Legacy NDC, 1 package rows	20200410_c4705321-8349-4fcd-b5e4-b30b855102d3.zip

Products#

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

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

MAMU Hand Sanitizer gel
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71909-0001	71909-0001-1

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
a2da64a5-de37-af8e-e053-2995a90ae453			c4705321-8349-4fcd-b5e4-b30b855102d3	2020-04-09	Warnings	Exact identifier spl id: a2da64a5-de37-af8e-e053-2995a90ae453 spl set id: c4705321-8349-4fcd-b5e4-b30b855102d3

Reported adverse events (FAERS/openFDA)#

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