DEB INSTANTFOAM ALCOHOL SANITIZER- ethyl alcohol liquid

Deb InstantFoam Alcohol Sanitizer by

Drug Labeling and Warnings

Deb InstantFoam Alcohol Sanitizer by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., SC Johnson Professional CA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 70% ww

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For hand sanitizing to reduce bacteria on the skin

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

Apply foaming sanitizer to cover hands

Rub into skin

No need to rinse

INACTIVE INGREDIENT

Inactive ingredients

AQUA (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.

PRINCIPAL DISPLAY PANEL

NDC: 11084-703-27

deb stoko

Deb InstantFOAM

Alcohol Hand Sanitizer
No Water Required | Kills 99.999% of Common Germs

Antiséptico para manos en espuma - con alcohol
No se requiere agua | Elimina el 99.999% de los gérmenes más
comunes

SANITIZE

1 L (33.8 FL OZ)

Stock #IFS1L

Deb USA, Inc., 1-800-248-7190, www.debgroup.com

Made in Canada, DCN9313 L-1251 R6

OPEN FOR DRUG FACTS

INGREDIENTS AND APPEARANCE

DEB INSTANTFOAM ALCOHOL SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-703
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-703-27	1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/2012
2	NDC: 11084-703-12	1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/2012
3	NDC: 11084-703-40	.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/2012
4	NDC: 11084-703-02	.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/15/2012

Labeler - SC Johnson Professional USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	manufacture(11084-703)