BZK Sanitizing Hand Wipe

Manufacturer
Premium PPE, LLC
Effective date
2021-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:49

Label at a glance#

ProductBZK Sanitizing Hand Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Cleans and sanitizes the skin and decreases bacteria. Recommended for single use.

Dosage and administration

Wipe liberally over the hands, rub into skin until dry. Recommended for single use.

Label contents#

Full prescribing information#

Directions for Use:

DOSAGE & ADMINISTRATION SECTION

Wipe liberally over the hands, rub into skin until dry. Recommended for single use.

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic/ hand and skin sanitizer

Uses:

INDICATIONS & USAGE SECTION

Cleans and sanitizes the skin and decreases bacteria. Recommended for single use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, L a u r e t h - 4 , P o l y h e x a n i d e , Phenoxyethanol, Trielhoxysilylpropyl
Steardimonium Chloride.

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.

Questions?

OTC - QUESTIONS SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81529-004-012023-01-30C16284748780-1f386c649-d087-0266-e053-dadaa90a7c1aBZK Sanitizing Hand Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81529-004-01BZK Sanitizing Hand Wipe1 in 1 PACKETCLOTH11
81529-004-01BZK Sanitizing Hand Wipe6.7 mL in 1 PATCHCLOTH6.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81529-004BZK SANITIZING HAND WIPE (BENZALKONIUM CHLORIDE) CLOTH [PREMIUM PPE, LLC]1Legacy NDC, 2 package rows20210310_bc2eae60-2bf4-2b2e-e053-2995a90af539.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
81529-00481529-004-01

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
bc2ea037-3dd0-5eca-e053-2a95a90a7f9dbc2eae60-2bf4-2b2e-e053-2995a90af5392021-02-25WarningsExact identifier
spl id: bc2ea037-3dd0-5eca-e053-2a95a90a7f9d
spl set id: bc2eae60-2bf4-2b2e-e053-2995a90af539

Reported adverse events (FAERS/openFDA)#

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