FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER - benzalkonium chloride solution
Fikes Northwest, Corp.

Non AlcoholFoaming Instant Hand Sanitizer

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

Warning

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. •

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. •

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pump a small amount of foam into palm of hand
Rub thoroughly over all surfaces of both hands
Rub hands together briskly until dry

Inactive Ingredients Water, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Principal Display Panel

Fikes Northwest

Non AlcoholFoaming Instant Hand Sanitizer

• Enhanced with Moisturizers

• Kills disease causing germs within seconds

• Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms

• Assists with OSHA Bloodborne Pathogen Standard Compliance

See side panel for additional information.

For Hospital and Professional Use Only

Net Contents: One Gallon (128 Fl. Oz.) 3.78 liters

FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER
husky 514 solution

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	50036-514
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride (benzalkonium)	benzalkonium chloride	1 g in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
water
dihydroxypropyl peg-5 linoleammonium chloride
glycereth-2 cocoate
behentrimonium chloride
dihydroxyethyl cocamine oxide

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	50036-514-05	3785 mL In 1 BOTTLE	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	11/16/2009

Labeler - Fikes Northwest, Corp. (167376284)

Registrant - Fikes Northwest, Corp. (167376284)

Establishment
Name	Address	ID/FEI	Operations
Canberra Corporation		068080621	MANUFACTURE

Revised: 01/2010Fikes Northwest, Corp.