FDA.reportPublic FDA data

Zoono Odor Guard

Manufacturer
ZOONO USA, LLC
Effective date
2017-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:16:33

Label at a glance#

ProductZoono Odor Guard
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

To prevent the growth of bacteria that cause body odor.

Dosage and administration

Spray on underarm and allow to air dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

DOSAGE & ADMINISTRATION SECTION

To prevent the growth of bacteria that cause body odor.

Warnings:

WARNINGS SECTION

For external use only.

WARNINGS SECTION

Do not use in the eyes

When using this product avoid contact with eyes. In case of eye contact flush eyes with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation and redness develop.

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:

INDICATIONS & USAGE SECTION

Spray on underarm and allow to air dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Ethyl alcohol, Fragrances, Silica Complex (3-Trimethoxysilyl Propyl Dimethyl Octadecyl Ammonium Chloride), Water

Questions?

OTC - QUESTIONS SECTION

Telephone 1-844-966-6687 Monday through Friday 8:00am till 5:00pm EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

typical label for all sizestypical label for all sizes

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69221-41069221-410-01, 69221-410-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
c055742d-60e2-1360-e053-2a95a90a46584522a13f-930f-2ff4-e054-00144ff8d46c2021-04-19WarningsExact identifier
spl set id: 4522a13f-930f-2ff4-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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