DMI Cosmetics Wash Me Hand Sanitizer

Manufacturer: DERMA INNOVATION COMPANY LIMITED
Effective date: 2020-05-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:13

Label at a glance#

ProductDMI Cosmetics Wash Me Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Storage and handling

Other information Store below 100°F (43°C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredients(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Anti-Bacterial, Antimicrobial and Germs

INDICATIONS & USAGE SECTION

Use(s) Hand Sanitizer Gel helps cleanse your hands instantly without rinse off. Gentle cleanses and nourishes your skin with all-round

protection.

WARNINGS SECTION

Warnings Flammable. Keep away from heat/ sparks/ open flames / hot surfaces.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Health & Safety Do not use on damaged, sensitive or irritated skin. Adult supervision advised for child use.

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Direction No water required. Apply to hands, rub in, ensuring contact with fingernails and in between fingers. Can also be applied to the body.

STORAGE AND HANDLING SECTION

Other information Store below 100°F (43°C) May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water, Glycerin, Aminomethylpropanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ammonium

Acryloyldimethyltaurate/VP Copolymer, Imidazolidinyl Urea

SPL UNCLASSIFIED SECTION

75% Alcohol

Product of Thailand

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IMAGE1IMAGE2IMAGE3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77586-001-01	2022-01-28	C162847	48780-1	d6a99b39-3e12-a426-e053-dadaa90af4c2	DMI COSMETICS WASH ME HAND SANITIZER
77586-001-02	2022-01-28	C162847	48780-1	d6a99b39-3e12-a426-e053-dadaa90af4c2	DMI COSMETICS WASH ME HAND SANITIZER
77586-001-03	2022-01-28	C162847	48780-1	d6a99b39-3e12-a426-e053-dadaa90af4c2	DMI COSMETICS WASH ME HAND SANITIZER
77586-001-04	2022-01-28	C162847	48780-1	d6a99b39-3e12-a426-e053-dadaa90af4c2	DMI COSMETICS WASH ME HAND SANITIZER
77586-001-05	2022-01-28	C162847	48780-1	d6a99b39-3e12-a426-e053-dadaa90af4c2	DMI COSMETICS WASH ME HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77586-001-01	DMI Cosmetics Wash Me Hand Sanitizer	30 mL in 1 TUBE	GEL	30	1
77586-001-02	DMI Cosmetics Wash Me Hand Sanitizer	50 mL in 1 TUBE	GEL	50	1
77586-001-03	DMI Cosmetics Wash Me Hand Sanitizer	400 mL in 1 BOTTLE, PUMP	GEL	400	1
77586-001-04	DMI Cosmetics Wash Me Hand Sanitizer	450 mL in 1 BOTTLE, PUMP	GEL	450	1
77586-001-05	DMI Cosmetics Wash Me Hand Sanitizer	1000 mL in 1 BOTTLE, PLASTIC	GEL	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77586-001	DMI COSMETICS WASH ME HAND SANITIZER (ALCOHOL) GEL [DERMA INNOVATION COMPANY LIMITED]	1	Legacy NDC, 5 package rows	20200516_565a61b4-c0ee-4182-a340-6d0716880be2.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

DMI Cosmetics Wash Me Hand Sanitizer
Alcohol
WATER
GLYCERIN
AMINOMETHYLPROPANOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
IMIDUREA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77586-001	77586-001-01, 77586-001-02, 77586-001-03, 77586-001-04, 77586-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	W59H9296ZG	IACT
IMIDUREA	M629807ATL	IACT

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
97d40577-2be7-40d6-b5c9-f33481bba3bc			565a61b4-c0ee-4182-a340-6d0716880be2	2020-05-12	Warnings	Exact identifier spl id: 97d40577-2be7-40d6-b5c9-f33481bba3bc spl set id: 565a61b4-c0ee-4182-a340-6d0716880be2

Reported adverse events (FAERS/openFDA)#

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