Zest Aqua Antibacterial Hand Soap

Zest Aqua Antibacterial Hand by

Drug Labeling and Warnings

Zest Aqua Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Abaco Partners LLC DBA Surefil. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZEST AQUA ANTIBACTERIAL HAND  ZEST- benzalkonium chloride soap 
Abaco Partners LLC DBA Surefil

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Zest Aqua Antibacterial Hand Soap

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.

Distributed By: High Ridge Brands, LLC. Stamford, CT 06902.

PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label

Clean Zestfully!

Zest

Antibacterial
LIQUID HAND SOAP

PLUS
VITAMIN E
& ALOE

FRESH AQUA

7.5 FL. OZ. (221 mL)

12P8003

PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label
ZEST AQUA ANTIBACTERIAL HAND   ZEST
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 20890-1794
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Product Characteristics
Colorblue (Aqua Blue) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 20890-1794-1221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/15/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/15/2014
Labeler - Abaco Partners LLC DBA Surefil (964809417)
Establishment
NameAddressID/FEIBusiness Operations
Abaco Partners LLC DBA Surefil964809417manufacture(20890-1794)

Revised: 1/2022
Document Id: d53e2d37-0f8a-6983-e053-2995a90af4cb
Set id: ac8bf24f-819b-4894-bc37-15ec63c439aa
Version: 3
Effective Time: 20220110