FDA.reportPublic FDA data

BZK Towelette

Manufacturer
Henry Schein Inc.
Effective date
2011-10-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:29:59

Label at a glance#

ProductBZK Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT:

 Benzalkonium Chloride, 0.133% w/v


OTC - PURPOSE SECTION

PURPOSE:

First Aid Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Caution Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

USE:  Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds.

WARNINGS SECTION

DO NOT USE: In the eyes or apply over large areas of the body.

STOP USE: If irritation, redness or other symptoms develop.  Consult a doctor if the condition persists or gets worse.

DOSAGE & ADMINISTRATION SECTION

Contains 1 Pad

DIRECTIONS: Tear open packet, unfold and use as washcloth

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT: Distilled Water

PRINCIPAL DISPLAY PANEL - Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HENRY SCHEIN®
112-5824

NDC 0404-5824-01

BZK
TOWELETTE

Contains Benzalkonium Chloride
For External Use Only
NON-STERILE

Contains
1 Pad

CE

Distributed by:

HENRY SCHEIN INC.
Melville, NY 11747 USA
EC REP

Henry Schein U.K. Holdings Ltd.
Gillingham ME8 0SB U.K.

Principal Display Panel - Pouch Label
Principal Display Panel - Pouch Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043307benzalkonium Cl 0.133 % Medicated PadPSN2
1043307benzalkonium chloride 1.33 MG/ML Medicated PadSCD2
1043307benzalkonium chloride 0.133 % Medicated ToweletteSY2
1043307benzalkonium chloride 0.133 % Topical SwabSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0404-5824-012020-01-31C16284748780-19d75b9cf-d52c-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0404-5824-01BZK Towelette1 mL in 1 POUCHSWAB12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0404-5824BZK TOWELETTE (BENZALKONIUM CHLORIDE) SWAB [HENRY SCHEIN INC.]2Legacy NDC, 1 package rows20111102_463a7d7f-9a1a-4434-b48d-efe331be26a6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W72
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y2
WATERINACTIVE INGREDIENT059QF0KO0R2

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
0404-58240404-5824-01

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIM
WATER059QF0KO0RIACT

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
47424e29-8f84-450e-9f13-89a130394660463a7d7f-9a1a-4434-b48d-efe331be26a62011-10-05WarningsExact identifier
spl id: 47424e29-8f84-450e-9f13-89a130394660
spl set id: 463a7d7f-9a1a-4434-b48d-efe331be26a6

Reported adverse events (FAERS/openFDA)#

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