HUSKY 514 NON-ALCOHOL FOAMING INSTANT HAND SANITIZER- husky 514 solution

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

HUSKY 514 Non-Alcohol Foaming Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by 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 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

Manufactured By:
CANBERRA CORPORATION
3610 Holland-Sylvania Rd.
Toledo, Ohio 43615

PRINCIPAL DISPLAY PANEL

Label Content for 128 Fl. Oz:

Husky®

514

NON-ALCOHOL FOAMING 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

PRINCIPAL DISPLAY PANEL

Label Content for 18.60 Fl. Oz:

Husky®

514

NON-ALCOHOL FOAMING 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: 18.60 fl. oz./550 mL.

PRINCIPAL DISPLAY PANEL

Label Content for 250 mL:

Husky

514

NON-ALCOHOL FOAMING 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: 250 mL

514-001-001-S01F

PRINCIPAL DISPLAY PANEL

Label Content for 1.69 Fl Oz:

Husky

514

NON-ALCOHOL FOAMING 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: 1.69 fl. Oz (50 mL)

INGREDIENTS AND APPEARANCE

HUSKY 514 NON-ALCOHOL FOAMING INSTANT HAND SANITIZER 
husky 514 solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63779-514
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: 63779-514-10	3785 mL in 1 BOTTLE
2	NDC: 63779-514-82	550 mL in 1 BOTTLE
3	NDC: 63779-514-99	250 mL in 1 BOTTLE
4	NDC: 63779-514-42	50 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 - Canberra Corporation (068080621)

Registrant - Canberra Corporation (068080621)

Establishment
Name	Address	ID/FEI	Business Operations
Canberra Corporation		068080621	MANUFACTURE