COVEX ANTIBACTERIAL LIQUID HAND WASH COOL PROTECTION- benzalkonium chloride liquid
DALAN KIMYA ENDUSTRI ANONIM SIRKETI

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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Covex Antibacterial Liquid Hand Wash Cool Protection

Drug Facts

Active ingredients

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only

When using this product.

Do not use

in the eyes.

Stop use and ask a doctor if

irritation and redness develop. if condition persists for more than 72 hours consult a doctor

Keep out of reach of children.

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

Directions

Wet hands and forearms. Apply 5 mililiters (teaspoonful) or palmful to hands and forearms. Scrub thoroughly for 60 seconds. Rinse and Repeat

Inactive ingredients:

Water, Cocamidopropyl Betaine, Lauryl Amine Oxide, Cocamine Oxide, Cocamidopropylamine Oxide, Sodium Chloride, Glycerine, Lactic Acid, Sodium Lactate, PEG-120 Methyl Glucose Dioleate, Fragrance, Laureth-7 Citrate, Tetrasodium EDTA, Triethylene Glycol, Propylene Glycol, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Linalool, Blue 1.

Package Labeling:

Label6

COVEX ANTIBACTERIAL LIQUID HAND WASH COOL PROTECTION
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51209-031
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID (UNII: 33X04XA5AT)
SODIUM LACTATE (UNII: TU7HW0W0QT)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
EDETATE SODIUM (UNII: MP1J8420LU)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51209-031-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	02/24/2021

Labeler - DALAN KIMYA ENDUSTRI ANONIM SIRKETI (566219285)