Active Ingredient
Ethyl Alcohol 70% w/w
Deb Med Instantfoam Optidose Hand Sanitizer
FDA Label NDC 11084-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Deb Usa, Inc. for the product Deb Med Instantfoam Optidose Hand Sanitizer (NDC 11084-200). 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, keep out of reach of children., directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
For hand sanitizing to reduce bacteria on skin
Warnings
For external use only
Flammable: Keep away from fire or flame.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply foaming sanitizer to cover dry hands
Rub into skin
No rinsing required
Inactive Ingredients
Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chloride.
Package Label.Principal Display Panel
deb med
Engineering Hand Hygiene Compliance
NDC 11084-200-27
optidose
InstantFOAM moisturing hand sanitizer
Certified EcoLogo
Certified Instant Hand Antiseptic CCD-170
USDA Certified Biobased Product
Made in Canada
US Patents 5,445,288 & 6,082,586
Worldwide Patent Pending.
Made by Deb for:
Deb USA, Inc.
Charlotte, NC 28217
1-800-248-7190
NSF
Nonfood Compounds Program Listed E3
140062
DMIFS1L
1 Liter 33.8 fl. oz.
Rev. 10-12
* Please review the disclaimer below.
