Zest Antibacterial Liquid Hand Soap, Fresh Aqua

Manufacturer: Sodalis USA, LLC
Effective date: 2025-02-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:55:33

Label at a glance#

ProductZest Antibacterial Liquid Hand Soap, Fresh Aqua

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

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.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	1
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	1
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	1
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81277-013-01	Zest Antibacterial Liquid Hand Soap, Fresh Aqua	221 mL in 1 BOTTLE, PUMP	GEL	221		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81277-013	ZEST ANTIBACTERIAL LIQUID HAND SOAP, FRESH AQUA (BENZALKONIUM CHLORIDE) GEL [SODALIS USA, LLC]	1	1 package rows	20250221_72ca863e-9872-45a5-b30d-e615339970d8.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Zest Antibacterial Liquid Hand Soap, Fresh Aqua
BENZALKONIUM CHLORIDE
WATER
CETRIMONIUM CHLORIDE
GLYCERIN
COCAMIDE MEA
LAURAMIDOPROPYLAMINE OXIDE
SODIUM CHLORIDE
PEG-120 METHYL GLUCOSE DIOLEATE
MYRISTAMIDOPROPYLAMINE OXIDE
CITRIC ACID MONOHYDRATE
EDETATE SODIUM
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE
METHYLCHLOROISOTHIAZOLINONE
FD&C GREEN NO. 3
METHYLISOTHIAZOLINONE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81277-013	81277-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
GLYCERIN	PDC6A3C0OX	IACT
COCAMIDE MEA	C80684146D	IACT
LAURAMIDOPROPYLAMINE OXIDE	I6KX160QTV	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
PEG-120 METHYL GLUCOSE DIOLEATE	YM0K64F20V	IACT
MYRISTAMIDOPROPYLAMINE OXIDE	3HSF539C9T	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
FD&C GREEN NO. 3	3P3ONR6O1S	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2e7120ac-b045-7cbb-e063-6294a90a19b3			72ca863e-9872-45a5-b30d-e615339970d8	2025-02-18	Warnings	Exact identifier spl id: 2e7120ac-b045-7cbb-e063-6294a90a19b3 spl set id: 72ca863e-9872-45a5-b30d-e615339970d8

Reported adverse events (FAERS/openFDA)#

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