FDA.reportPublic FDA data

Defense Zone

Manufacturer
Prime Enterprises, Inc.
Effective date
2022-04-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:04:23

Label at a glance#

ProductDefense Zone Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Wet hands, work into a rich lather Rinse well For children under 6, use only under adult supervision

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop

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, work into a rich lather

Rinse well

For children under 6, use only under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/Beheneth-25 Mathacrylate/HEMA Crosspolymer-2, Aloe Barbadensis Leaf Juice, Camellia Oleifera (Green Tea) Leaf Extract, Cetrimonium Chloride, Citric Acid, Cocamide DIPA, Ethylhexylglycerin, Fragrance, Glycerin, Lauramine Oxide, PEG-150 Distearate, Phenoxyethanol, Red 40, Tetrasodium Glutamate Diacetate, Water, Yellow 5

Defense Zone Antibacterial Hand Soap Fresh Peach

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display LabelPrincipal Display Label

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
58443-037958443-0379-5

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PEG-150 DISTEARATE6F36Q0I0ACIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
COCO DIISOPROPANOLAMIDES485AM948QIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FD&C RED NO. 40WZB9127XOAIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
CAMELLIA OLEIFERA LEAF5077EL0C60IACT
WATER059QF0KO0RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
dbe949c1-dead-54f3-e053-2a95a90a6a5db82b3210-8eee-dcaa-e053-2995a90a285f2022-04-05WarningsExact identifier
spl id: dbe949c1-dead-54f3-e053-2a95a90a6a5d
spl set id: b82b3210-8eee-dcaa-e053-2995a90a285f

Reported adverse events (FAERS/openFDA)#

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