FDA.reportPublic FDA data

Zest Aqua Antibacterial Hand

Manufacturer
Abaco Partners LLC DBA Surefil
Effective date
2022-01-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:18:41

Label at a glance#

ProductZest Aqua Antibacterial Hand Zest
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

wet hands apply to palm of hand scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

INDICATIONS & USAGE SECTION

Uses for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only - hands only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands
  • apply to palm of hand
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

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.

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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
PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
20890-1794-12024-01-30C16284748780-11030e365-4a6e-111a-e063-dadaa90a10e2Zest Aqua Antibacterial Hand Soap

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20890-179420890-1794-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
COCO MONOETHANOLAMIDEC80684146DIACT
SODIUM CHLORIDE451W47IQ8XIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C GREEN NO. 33P3ONR6O1SIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d53e2d37-0f8a-6983-e053-2995a90af4cbac8bf24f-819b-4894-bc37-15ec63c439aa2022-01-10WarningsExact identifier
spl id: d53e2d37-0f8a-6983-e053-2995a90af4cb
spl set id: ac8bf24f-819b-4894-bc37-15ec63c439aa

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.