Active Ingredient
Ethyl Alcohol, 80%
Dreumex Omnicare Hand Sanitizer
FDA Label NDC 53305-065
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dreumex Usa, Inc. for the product Dreumex Omnicare Hand Sanitizer (NDC 53305-065). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor, contents under pressure., keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
For hand cleaning to decrease bacteria on the skin.
Recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from fire or flame. No Smoking.
When Using This Product
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
if irritation or redness develops.
Contents Under Pressure.
Do not puncture or incinerate. Do not store at temperatures above 120°F (50°C).
Keep Out Of Reach Of Children.
If swallowed get medical help, or contact a poison control center immediately.
Directions
- apply a palmful to hands
- scrub thoroughly until dry
Inactive Ingredients
water panthenol, glycerin, cetyl alcohol, propylene glycol.
For Questions Or Comments
or to report any adverse reactions or side effects, please call 1-800-233-9382.
Principal Display Panel -- Label On Individual Unit Can
Container Label (Hand Sanitizer Spray)
* Please review the disclaimer below.
