BZK Alcohol Free Hand Sanitizer

Manufacturer
Premium PPE, LLC
Effective date
2021-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:50

Label at a glance#

ProductBZK Alcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

BZK™ Alcohol Free Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use.

Dosage and administration

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Hand & Skin Sanitizer

Uses:

INDICATIONS & USAGE SECTION

BZK™ Alcohol Free Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use.

Warnings:

WARNINGS SECTION

Do not freeze

+ For external use only 

Do not use

OTC - DO NOT USE SECTION

+ in ears, eyes or mouth

When using this product,

OTC - WHEN USING SECTION

+avoid contact with the eyes

+ In case of contact, flush eyes with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

+redness or irritation develops and persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

+Children should be supervised when using this product.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.

Other Information:

SPL UNCLASSIFIED SECTION

Store in a cool dry place below 104°F(40°C).

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

OTC - QUESTIONS SECTION

1-800-920-7650 Mon-Fri 10AM-4PM (EST)

Package Labeling:150ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Package Labeling:50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD1
1049254benzalkonium chloride 0.13 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81529-002-01BZK Alcohol Free Hand Sanitizer50 mL in 1 BOTTLELIQUID501
81529-002-02BZK Alcohol Free Hand Sanitizer150 mL in 1 BOTTLELIQUID1501
81529-002-03BZK Alcohol Free Hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81529-002BZK ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [PREMIUM PPE, LLC]1Legacy NDC, 3 package rows20210310_bd07aa82-c3b4-1da3-e053-2995a90a6b79.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81529-00281529-002-02, 81529-002-01, 81529-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
bd07a9e9-2a97-1cef-e053-2995a90a6ceabd07aa82-c3b4-1da3-e053-2995a90a6b792021-03-08WarningsExact identifier
spl id: bd07a9e9-2a97-1cef-e053-2995a90a6cea
spl set id: bd07aa82-c3b4-1da3-e053-2995a90a6b79

Reported adverse events (FAERS/openFDA)#

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