EVERGREEN- benzalkonium chloride cloth

Evergreen by

Drug Labeling and Warnings

Evergreen by is a Otc medication manufactured, distributed, or labeled by ELA KOZMETIK VE HIJYENIK URUNLERI SANAYI TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Uses

hand sanitizer to decrease bacteria on the skin

recommended for repeated use

for use when soap and water are not available

Warnings

For external use only

Do not use

on children less than 2 years of age

on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

irritation and redness develop

condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping

supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F)

avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

water, phenoxyethanol, benzoic acid, dehydroacetic acid, cetearyl isononanoate, ceteareth-20, cetearyl alcohol, glyceryl stearate, ceteareth-12, cetyl palmitate, cocamidopropyl betaine, fragrance, glycerin, tetrasodium EDTA, allantoin, panthenol, disodium laureth sulfosuccinate

SPL UNCLASSIFIED SECTION

MAXIMUM PROTECTION

LEMON SCENTED

pH BALANCED

GENTLE ON SKIN

DERMATOLOGIST TESTED

ALCOHOL & PARABEN FREE

*KILLS 99% OF MOST COMMON GERMS & BACTERIA THAT MAY CAUSE ILLNESS

To Dispense Wipe:

* Flip open the dispensing cap

* Peel back the security label

* Remove wipes

To reseal the package: Slightly press on the dispensing cap

Imported By:

Evergreen USA LLC

Hoboken, NJ 07030

www.egreenusa.com

PRODUCT OF TURKEY

Packaging

INGREDIENTS AND APPEARANCE

EVERGREEN 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79881-020
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 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
CETEARYL ISONONANOATE (UNII: P5O01U99NI)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETEARETH-12 (UNII: 7V4MR24V5P)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
ALLANTOIN (UNII: 344S277G0Z)
PANTHENOL (UNII: WV9CM0O67Z)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79881-020-01	20 in 1 PACKET	04/01/2020
1		2.964 g in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - ELA KOZMETIK VE HIJYENIK URUNLERI SANAYI TICARET LIMITED SIRKETI (356070214)

Establishment
Name	Address	ID/FEI	Business Operations
ELA KOZMETIK VE HIJYENIK URUNLERI SANAYI TICARET LIMITED SIRKETI		356070214	manufacture(79881-020)