EVERGREEN FRENCH LAVENDER SCENTED ANTIBACTERIAL HANDSOAP- benzalkonium chloride liquid

Evergreen French Lavender Scented Antibacterial Handsoap by

Drug Labeling and Warnings

Evergreen French Lavender Scented Antibacterial Handsoap by is a Otc medication manufactured, distributed, or labeled by GENC GIDA KOZMETIK VE KIMYASAL URUNLER SANAYI VE TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

INDICATIONS & USAGE

Uses  For handwashing to decrease bacteria on the skin

WARNINGS

Warnings For external use only

When using this product  Avoid contact with eyes. In case of eye contact, flush with water.

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pump into hands, wet as needed

Lather vigorously for at least 15 seconds

Wash skin, rinse thoroughly and dry

Inactive ingredients

Water, Sodium Laureth Sulfate, Cocamide MIPA, Sodium Chloride, Cocamidopropyl Betaine, Glycerin, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, CI 42090 (Blue 1), CI 17200 (Red 33)

SPL UNCLASSIFIED SECTION

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Imported By:

Evergreen USA LLC

Hoboken, NJ 07030

www.egreenusa.com

PRODUCT OF TURKEY

Packaging

INGREDIENTS AND APPEARANCE

EVERGREEN FRENCH LAVENDER SCENTED ANTIBACTERIAL HANDSOAP 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74600-504
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74600-504-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - GENC GIDA KOZMETIK VE KIMYASAL URUNLER SANAYI VE TICARET LIMITED SIRKETI (356827969)

Establishment
Name	Address	ID/FEI	Business Operations
GENC GIDA KOZMETIK VE KIMYASAL URUNLER SANAYI VE TICARET LIMITED SIRKETI		356827969	manufacture(74600-504)