FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER- husky 514 solution 
Fikes Northwest, Corp.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Non AlcoholFoaming Instant Hand Sanitizer

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

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

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

Package Label
FIKES NORTHWEST NON-ALCOHOL FOAMING INSTANT HAND SANITIZER 
husky 514 solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50036-514
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride1 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50036-514-053785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33311/16/2009
Labeler - Fikes Northwest, Corp. (167376284)
Registrant - Fikes Northwest, Corp. (167376284)
Establishment
NameAddressID/FEIBusiness Operations
Canberra Corporation068080621MANUFACTURE

Revised: 1/2010
Document Id: a1c2ade4-3511-4214-be58-9da4c5eb3108
Set id: 648eda6b-d897-4ab2-93f5-ed6954326c7c
Version: 1
Effective Time: 20100108
 
Fikes Northwest, Corp.