NATIVE GREEN FOAMING HAND SANITIZER- benzalkonium chloride solution

Native Green Foaming Hand Sanitizer by

Drug Labeling and Warnings

Native Green Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Native Green, Canberra Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient:

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin

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 – Bottle Label

NATIVE GREEN
FOAMING HAND SANITIZER
ALCOHOL-FREE – WITH MOISTURIZERS

Cleaner, Greener

SEE SIDE PANEL FOR ADDITIONAL INFORMATION.

INGREDIENTS AND APPEARANCE

NATIVE GREEN FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50409-514
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: 50409-514-82	550 mL in 1 BOTTLE
2	NDC: 50409-514-42	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	04/21/2010

Labeler - Native Green (791610038)

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