Zoono Foot Guard

Manufacturer: Zoono USA, LLC | Holly Oak Chemical, Inc
Effective date: 2020-12-15
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 23:01:53

Label at a glance#

ProductZoono Foot Guard

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

Spray liberally on feet, rub until dry. Do not used if allergic to any of the ingredients.

Contacts and useful links#

PhoneLabel contact1-844-966-6687

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Banzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use in the eyes.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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 Cener right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray liberally on feet, rub until dry. Do not used if allergic to any of the ingredients.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl Alcohol, Fragrance, Silica Complex 3-(Trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, Water

Questions or Comments?

OTC - QUESTIONS SECTION

Telephone: 1-844-966-6687

Monday through Friday

8:00am till 5:00pm EST

Primary Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

typical of all size packages

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Zoono Foot Guard
Benzalkonium Chloride
WATER
ALCOHOL
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69221-401	69221-401-01, 69221-401-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	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
c055200b-9d18-59c8-e053-2995a90af920			42ae8678-6489-6ce7-e054-00144ff88e88	2021-04-19	Warnings	Exact identifier spl set id: 42ae8678-6489-6ce7-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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