ELLE ANTIBACTERIAL HAND WASH- benzalkonium chloride liquid

ELLE ANTIBACTERIAL HAND WASH by

Drug Labeling and Warnings

ELLE ANTIBACTERIAL HAND WASH by is a Otc medication manufactured, distributed, or labeled by Alta Sales Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

Active Ingredient: Benzalkonium Chloride 0.24%

PURPOSE

​Purpose: Antiseptic

INDICATIONS & USAGE

Use 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 DRY hands
Lather vigorously for at least 15 seconds
Rinse and dry thoroughly

INACTIVE INGREDIENT

Inactive Ingredients: Water, Lauramine Oxide, Cetrimonium Chloride, Peg-150 Distearate, Coco Glucoside, Glyceryl Oleate, Tetrasodium Edta, Glycerin, Parfum, Citric Acid, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone.

SPL UNCLASSIFIED SECTION

Dermatologically Tested

Paraben Free

Hypoallergenic

Cruelty Free

ELLE™ is used by Alta Sales Inc under license from HACHETTE FILIPACCHI PRESSE SA, Paris, France.
Made in Turkey
www.ellepersonalcare.us

Packaging

INGREDIENTS AND APPEARANCE

ELLE ANTIBACTERIAL HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79165-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.24 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
EDETATE SODIUM (UNII: MP1J8420LU)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79165-112-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/03/2020

Labeler - Alta Sales Inc (080087931)