DERMA-GLOVE HAND SANITIZER GEL

Manufacturer: RWM TECHNOLOGIES
Effective date: 2010-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:25:11

Label at a glance#

ProductDerma-Glove

Active ingredientEthanol, Triclosan

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1-888-300-1225

Label contents#

Full prescribing information#

DESCRIPTION SECTION

DERMA-GLOVE(R) no rinse hand sanitizer gel

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethanol 60%..................................................................Antimicrobial

Triclosan 0.3%..............................................................Antiseptic

OTC - PURPOSE SECTION

Antiseptic/Antimicrobial hand sanitizer gel

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease
Recommended for repeated use

WARNINGS AND PRECAUTIONS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
Rinse with water after use
Children under 6 years of age should be supervised when using this product

GENERAL PRECAUTIONS SECTION

Do not store above 110^o F (43^o C)
For additional information, see Material Safety Data Sheet (MSDS).

INACTIVE INGREDIENT SECTION

Deionized Water, Glycereth-18 Ethylhexanoate, Glycereth-18, Polyoxyethylene (20) Sorbitan Monooleate, 2-Amino-2-methyl-1-propanol, Acrylate crosspolymer, Polyquaternium-69, Citric Acid and Sodium Citrate

OTC - QUESTIONS SECTION

Questions or Comments?

Call 1-888-300-1225 Monday through Friday 8:00 AM to 5:00 PM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL FILELABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
24673-248-01	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-02	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-03	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-04	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-05	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-06	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-07	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL
24673-248-08	2019-10-21	C162847	48780-1	956f9ecf-d602-621f-e053-dbdaa90a74ad	DERMA-GLOVE HAND SANITIZER GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
24673-248-01	Derma-Glove	55.2 g in 1 BOTTLE, PUMP	GEL	55.2	3
24673-248-02	Derma-Glove	110.4 g in 1 BOTTLE, PUMP	GEL	110.4	3
24673-248-03	Derma-Glove	220.8 g in 1 BOTTLE, PUMP	GEL	220.8	3
24673-248-04	Derma-Glove	3532.8 g in 1 BOTTLE, PUMP	GEL	3532.8	3
24673-248-05	Derma-Glove	17664 g in 1 DRUM	GEL	17664	3
24673-248-06	Derma-Glove	194304 g in 1 DRUM	GEL	194304	3
24673-248-07	Derma-Glove	883200 g in 1 DRUM	GEL	883200	3
24673-248-08	Derma-Glove	1236480 g in 1 DRUM	GEL	1236480	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
24673-248	DERMA-GLOVE (ETHANOL, TRICLOSAN) GEL [RWM TECHNOLOGIES]	3	Legacy NDC, 8 package rows	20100714_0945b0a3-7f95-430d-b606-16832adacfd5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Ethanol	ACTIVE INGREDIENT	3K9958V90M	3
Triclosan	ACTIVE INGREDIENT	4NM5039Y5X	3
Ethanol	ACTIVE MOIETY	3K9958V90M	3
Triclosan	ACTIVE MOIETY	4NM5039Y5X	3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Derma-Glove
Ethanol, Triclosan
Ethanol
Triclosan

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
24673-248	24673-248-01, 24673-248-02, 24673-248-03, 24673-248-04, 24673-248-05, 24673-248-06, 24673-248-07, 24673-248-08

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
Ethanol	3K9958V90M	ACTIB
Triclosan	4NM5039Y5X	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
77453def-d7fa-4cb6-8aaa-58c41de3cb58			0945b0a3-7f95-430d-b606-16832adacfd5	2010-06-01	Warnings	Exact identifier spl id: 77453def-d7fa-4cb6-8aaa-58c41de3cb58 spl set id: 0945b0a3-7f95-430d-b606-16832adacfd5

Reported adverse events (FAERS/openFDA)#

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