KOSETTE CARE SANITIZER- benzalkonium chloride spray

Kosette Care Sanitizer by

Drug Labeling and Warnings

Kosette Care Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kosette, MSP CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzalkonium chloride (0.135%)

Purpose

Antiseptic

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Uses

To decrease bacteria on the skin when soap and water are not available. Recommended for repeated use.

Warnings

For external use only

When using this product avoid contact with eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if skin irritation or redness develops and lasts.

Keep out of reach of children. If swallowed get medical help or contact a poison control center immediately.

Directions

Spray adequate amount to desired area (clothing or body) at a distance of 6 inches for best result. Avoid spraying onto dark colored clothing.

Inactive Ingredients

Quercus acutissima Sap, Water (Aqua), 1,2-Hexanediol, Propylene Glycol, PEG-60 Hydrogenated Castor Oil, Triethanolamine, Citric Acid, Fragrance (Parfum).

Kosette Care Sanitizer Spray

INGREDIENTS AND APPEARANCE

KOSETTE CARE SANITIZER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79369-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.135 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
QUERCUS ACUTISSIMA WHOLE (UNII: 0TVP714IPW)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
TROLAMINE (UNII: 9O3K93S3TK)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79369-100-01	80 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/29/2020

Labeler - Kosette (011133801)

Establishment
Name	Address	ID/FEI	Business Operations
MSP CO., LTD		695013758	manufacture(79369-100)