FDA Label for Deb Med Instantfoam Optidose Hand Sanitizer
View Indications, Usage & Precautions
Deb Med Instantfoam Optidose Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Deb Usa, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Ethyl Alcohol 70% w/w
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.