PROFORMANCE SERIES FOAM ALCOHOL HAND SANITIZER- ethyl alcohol liquid

ProFormance Series Foam Alcohol Hand Sanitizer by

Drug Labeling and Warnings

ProFormance Series Foam Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Pro-Link, Inc., Deb USA, Inc., Deb Worldwide Healthcare Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 72%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For hand sanitizing to reduce bacteria on 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 one shot of foaming sanitizer to dry hands

Rub into skin

No rinsing required

INACTIVE INGREDIENT

Inactive ingredients

Water, n-Propanol, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonim Chloride

PRINCIPAL DISPLAY PANEL

ProFormance Series

Foam Alcohol Sanitizer

Pro-Link Green

Certified EcoLogo

Certified Instant Hand Antiseptic CCD-170

MSA1000

Distributed exclusively by:

Pro-Link, Inc.

1 Liter

33.8 Fluid Ounces

INGREDIENTS AND APPEARANCE

PROFORMANCE SERIES FOAM ALCOHOL HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66908-107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
PROPYL ALCOHOL (UNII: 96F264O9SV)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66908-107-27	1000 mL in 1 BOTTLE, PLASTIC
2	NDC: 66908-107-12	1000 mL in 1 BOTTLE, PLASTIC

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

Labeler - Pro-Link, Inc. (144650637)

Registrant - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb Worldwide Healthcare Inc.		205662831	manufacture