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DEB MED INSTANTFOAM HAND SANITIZER- ethyl alcohol liquid
Deb USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antibacterial

Uses

For hand sanitizing to reduce bacterial on skin

Warnings

For external use only

Flammable: Keep away from fire or flame

When using this product avoid contact with eyes.

In case of eye contact, flush with water.

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-Clucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chloride.

deb med Engineering Hand Hygiene Compliance

InstantFOAM Moisturizing Hand Sanitizer

NDC: 11084-068-27

Certified EcoLogo

USDA Certified BioBased Product

NSF

Nonfood Compounds Program Listed E3

33.8 fl oz

DMIFS1LR

Rev. 01-13

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

www.debmed.com

DEB MED INSTANTFOAM HAND SANITIZER
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-068
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
PROPYL ALCOHOL (UNII: 96F264O9SV)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIMETHICONE (UNII: 92RU3N3Y1O)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)
PEG-200 DILAURATE (UNII: TWV5J70L88)
GLYCERYL COCOATE (UNII: WVK1CT5994)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 11084-068-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2011	10/01/2019
2	NDC: 11084-068-40	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2011	03/01/2019
3	NDC: 11084-068-01	47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2011	11/01/2019
4	NDC: 11084-068-12	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2011	11/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	02/01/2011	11/01/2019

Labeler - Deb USA, Inc. (607378015)

Name	Address	ID/FEI	Business Operations
Establishment
Deb Worldwide Healthcare Inc.		205662831	manufacture(11084-068)

Revised: 10/2017

Document Id: 4cba2741-738b-4fe9-876a-78e7c5791cfe

Set id: f64731f6-328d-4de1-9602-340b718f654e

Version: 6

Effective Time: 20171025

Deb USA, Inc.

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