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

Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

Fikes Northwest Non-Alcohol Foaming Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Fikes Northwest, Corp., Canberra Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y)	benzalkonium chloride	1 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
dihydroxypropyl peg-5 linoleammonium chloride (UNII: 0Y0NQR2GH1)
glycereth-2 cocoate (UNII: JWM00VS7HC)
behentrimonium chloride (UNII: X7GNG3S47T)
dihydroxyethyl cocamine oxide (UNII: 8AR51R3BL5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50036-514-05	3785 mL in 1 BOTTLE

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	Business Operations
Canberra Corporation		068080621	MANUFACTURE