GUNK GETTER SANITIZING- benzalkonium chloride spray

Gunk Getter Sanitizing by

Drug Labeling and Warnings

Gunk Getter Sanitizing by is a Otc medication manufactured, distributed, or labeled by PeerBasics LLC, Hangzhou Huiji Biotechnology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

• apply to hands.
• allow skin to dry without wiping.
• children under 2 years: ask a doctor before use.

Other information

• do not store above 105F(41C).
• may discolor some fabrics.
• harmful to wood finishes and plastics.

Inactive Ingredients

Water

Glycerol

Fungicide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GUNK GETTER SANITIZING 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83590-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) (LAURAMIDOPROPYLAMINE OXIDE - UNII:I6KX160QTV)	LAURAMIDOPROPYLAMINE OXIDE	1.5 mg  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83590-002-01	80 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2023
2	NDC: 83590-002-02	98 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2023
3	NDC: 83590-002-03	473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2023
4	NDC: 83590-002-04	828 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2023
5	NDC: 83590-002-05	946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/20/2023

Labeler - PeerBasics LLC (087291627)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co.,Ltd		526893497	manufacture(83590-002)