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Native Green Foaming Hand Sanitizer

Medically reviewed on April 2, 2018

Dosage form: solution
Ingredients: benzalkonium chloride 1g in 1000mL
Labeler: Native Green
NDC Code: 50409-514

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.

Drug Facts

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.

NATIVE GREEN FOAMING HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50409-514
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (benzalkonium) benzalkonium chloride1 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
water 
dihydroxypropyl peg-5 linoleammonium chloride 
glycereth-2 cocoate 
behentrimonium chloride 
dihydroxyethyl cocamine oxide 
Packaging
#Item CodePackage Description
1NDC:50409-514-82550 mL in 1 BOTTLE
2NDC:50409-514-4250 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33304/21/2010
Labeler - Native Green (791610038)
Establishment
NameAddressID/FEIOperations
Canberra Corporation068080621MANUFACTURE

 
Native Green

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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