COVEX ANTIBACTERIAL HAND WASH ACTIVE PROTECTION- benzalkonium chloride liquid

Covex Antibacterial Hand Wash Active Protection by

Drug Labeling and Warnings

Covex Antibacterial Hand Wash Active Protection by is a Otc medication manufactured, distributed, or labeled by DALAN KIMYA ENDUSTRI ANONIM SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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, Limonene, Yellow 5, Red 40.

Package Labeling:

INGREDIENTS AND APPEARANCE

COVEX ANTIBACTERIAL HAND WASH ACTIVE PROTECTION 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51209-030
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51209-030-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2021

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

Labeler - DALAN KIMYA ENDUSTRI ANONIM SIRKETI (566219285)