ZEST ANTIBACTERIAL LIQUID HAND SOAP, FRESH AQUA- benzalkonium chloride gel

Zest Antibacterial Liquid Hand Soap, Fresh Aqua by

Drug Labeling and Warnings

Zest Antibacterial Liquid Hand Soap, Fresh Aqua by is a Otc medication manufactured, distributed, or labeled by Sodalis USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only- hands only

When using this product

 avoid contact with the eyes. If contact occurs, rinse eyes 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

 wet hands

 apply to palm of hand

 scrub thoroughly

 rinse thoroughly

Inactive ingredients:

Water, Cetrimonium Chloride, Glycerin, Cocamide MEA, Lauramidopropylamine Oxide, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Myristamidopropylamine Oxide, Citric Acid, Fragrance, Tetrasodium EDTA, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylchloroisothiazolinone, Green 3, Methylisothiazolinone.

Package Labeling:

INGREDIENTS AND APPEARANCE

ZEST ANTIBACTERIAL LIQUID HAND SOAP, FRESH AQUA 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81277-013
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)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDE MEA (UNII: C80684146D)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81277-013-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/15/2020

Labeler - Sodalis USA, LLC (119375257)