Dreumex Omnicare Hand Sanitizer

Manufacturer: Dreumex USA, Inc. | BiB Production and Packaging B.V.
Effective date: 2018-09-05
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-05-31 22:56:44

Label at a glance#

ProductDreumex Omnicare Hand Sanitizer

Active ingredientALCOHOL

Label structure13 sections

Indications and uses

For hand cleaning to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

apply a palmful to hands scrub thoroughly until dry

Storage and handling

Do not puncture or incinerate. Do not store at temperatures above 120°F (50°C).

Contacts and useful links#

PhoneLabel contact1-800-233-9382

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 80%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand cleaning to decrease bacteria on the skin.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame. No Smoking.

When using this product

OTC - WHEN USING SECTION

avoid contact with face, eyes and broken skin. If eye contact occurs, rinse eyes thoroughly with water and seek medical advice.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or redness develops.

Contents under pressure.

STORAGE AND HANDLING SECTION

Do not puncture or incinerate. Do not store at temperatures above 120°F (50°C).

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help, or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

apply a palmful to hands
scrub thoroughly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water panthenol, glycerin, cetyl alcohol, propylene glycol.

For questions or comments

OTC - QUESTIONS SECTION

or to report any adverse reactions or side effects, please call 1-800-233-9382.

Principal Display Panel -- Label on individual unit can

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Container Label

Carton Label -- package of 6 cans

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53305-065-02	2020-01-31	C162847	48780-1	9d75b9d0-3829-f424-e053-dadaa90a57ce	ecc8ee22-cf81-4964-80d3-79711875428e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53305-065-01	Dreumex Omnicare Hand Sanitizer	400 mL in 1 CAN	SPRAY	400		7
53305-065-02	Dreumex Omnicare Hand Sanitizer	6 in 1 CASE	SPRAY	6		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53305-065	DREUMEX OMNICARE HAND SANITIZER (ALCOHOL) SPRAY [DREUMEX USA, INC.]	7	Legacy NDC, 2 package rows	20180906_ecc8ee22-cf81-4964-80d3-79711875428e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	3
ALCOHOL	ACTIVE MOIETY	3K9958V90M	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	3

Products#

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

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

Dreumex Omnicare Hand Sanitizer
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53305-065	53305-065-01, 53305-065-02

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
673ce252-175b-2ccb-e053-2a91aa0afc11			ecc8ee22-cf81-4964-80d3-79711875428e	2018-09-05	Warnings	Exact identifier spl id: 673ce252-175b-2ccb-e053-2a91aa0afc11 spl set id: ecc8ee22-cf81-4964-80d3-79711875428e

Reported adverse events (FAERS/openFDA)#

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