BZK Agent Sanitizer

Manufacturer
Tropical Enterprises International, Inc.
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:22

Label at a glance#

ProductBZK Agent Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Benzalkonium Chloride 0.13%

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops and persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeat use.

OTC - QUESTIONS SECTION

Questions: 1-800-535-5053

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and persists.

OTC - WHEN USING SECTION

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

DOSAGE & ADMINISTRATION SECTION

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Directions: Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 2-Phenoxyethanol, Silicon Quaternary Ammonia Salt .75%

WARNINGS SECTION

WARNINGS For external use only

SAFE HANDLING WARNING SECTION

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

OTHER SAFETY INFORMATION

Other info: Non-staining, may discolor certain fabrics.

INDICATIONS & USAGE SECTION

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeat use.

Directions: Wet hands thoroughly with product and allow to dry without wiping.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58418-759-082022-01-28C16284748780-1d6a99b39-9b96-a426-e053-dadaa90af4c2Non-Alcohol Sanitizer spray with Spar Additive.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58418-759-08BZK Agent Sanitizer240 mL in 1 BOTTLE, SPRAYSPRAY2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58418-759BZK AGENT SANITIZER (NON ALCOHOL SPRAY SANITIZER WITH ADDITIVE) SPRAY [TROPICAL ENTERPRISES INTERNATIONAL, INC.]1Legacy NDC, 1 package rows20210101_b7cb06ca-8b20-548e-e053-2995a90a73d7.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58418-75958418-759-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
b7cb06ca-8b21-548e-e053-2995a90a73d7b7cb06ca-8b20-548e-e053-2995a90a73d72020-12-31WarningsExact identifier
spl id: b7cb06ca-8b21-548e-e053-2995a90a73d7
spl set id: b7cb06ca-8b20-548e-e053-2995a90a73d7

Reported adverse events (FAERS/openFDA)#

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