GUNK GETTER SANITIZING- benzalkonium chloride spray 
PeerBasics LLC

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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Active Ingredient

Benzalkonium Chloride

Lauramide Propyl Dimethyl Oxide Amine

Purpose

Antimicrobial Agent

Surfactant

Antifugal

Use

Use to decrase bacteria on the skin.

Warnings

For external use only

Do not use

Do not use it you are allergic to any of the ingredients.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin.
  • do not inhale or ingest.

Stop use and ask a doctor if

irritation or rash develops and continues for more than72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 years and over:

Other information

Inactive Ingredients

Water

Glycerol

Fungicide

Label

GUNK GETTER SANITIZING 
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83590-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) (LAURAMIDOPROPYLAMINE OXIDE - UNII:I6KX160QTV) LAURAMIDOPROPYLAMINE OXIDE1.5 mg  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83590-002-0180 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/20/2023
2NDC:83590-002-0298 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/20/2023
3NDC:83590-002-03473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/20/2023
4NDC:83590-002-04828 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/20/2023
5NDC:83590-002-05946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/20/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/20/2023
Labeler - PeerBasics LLC (087291627)
Establishment
NameAddressID/FEIBusiness Operations
Hangzhou Huiji Biotechnology Co.,Ltd526893497manufacture(83590-002)

Revised: 8/2023
Document Id: 03a6805e-6599-ef81-e063-6294a90ad65b
Set id: 00e75912-7225-114c-e063-6294a90ab9aa
Version: 2
Effective Time: 20230824
 
PeerBasics LLC