DEB INSTANTFOAM COMPLETE- alcohol liquid

Deb InstantFOAM Complete by

Drug Labeling and Warnings

Deb InstantFOAM Complete 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

ETHYL ALCOHOL, 80% w/w

Purpose

Antibacterial

Uses

for hand sanitizing to reduce bacteria on the 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 hands

rub into skin

no rinsing required

Inactive ingredients

AQUA (WATER), BIS-PEG-12 DIMETHICONE, CITRIC ACID, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PANTHENOL, PEG-200 HYDROGENATED GLYCERYL PALMITATE, PEG-7 GLYCERYL COCOATE

PRINCIPAL DISPLAY PANEL

deb stoko

NDC: 11084-170-27

Deb InstantFOAM Complete

EN Broad Spectrum Alcohol-Based Instant Hand Sanitizer Foam with Moisturizer and Skin Conditioner

Perfume-free   Dye-free   No water required  Kills 99.999% of many types of common germs

ES Amplio espectro antiseptico con alcohol para manos en espuma y con acondicionador

Sin perfume   Sin colorante   No se requiere agua   Elimina el 99.999% de los muchos tipos de germenes mas comunes

SANITIZE

deb

Stock #:

IFC1L

Made in / Hecho en 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.debgroup.com

DCN9207/0715

1 L

(33.8 fl oz)

Meets food code hand sanitizer criteria (Section 2-301.16) published by the FDA

INGREDIENTS AND APPEARANCE

DEB INSTANTFOAM COMPLETE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-170
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.80 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCO GLUCOSIDE (UNII: ICS790225B)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
GLYCERYL OLEATE (UNII: 4PC054V79P)
PANTHENOL (UNII: WV9CM0O67Z)
PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-170-01	47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/18/2015
2	NDC: 11084-170-40	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/18/2015
3	NDC: 11084-170-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/18/2015
4	NDC: 11084-170-12	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/18/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/18/2015

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

Registrant - SC Johnson Professional USA, Inc. (078805627)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	manufacture(11084-170)