BZK Towelette

Manufacturer
Acme United Corporation
Effective date
2019-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:12

Label at a glance#

ProductBZK Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.133% w/v

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Do Not Use

OTC - DO NOT USE SECTION

In the eyes or apply over large areas of the body.

Stop Use

OTC - STOP USE SECTION

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

Caution

WARNINGS SECTION

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, unfold and use as a washcloth.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Bicarbonate, Water

Principal Display Panel - 1.4 mL Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton ImageCarton ImageCarton Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043307benzalkonium Cl 0.133 % Medicated PadPSN1
1043307benzalkonium chloride 1.33 MG/ML Medicated PadSCD1
1043307benzalkonium chloride 0.133 % Medicated ToweletteSY1
1043307benzalkonium chloride 0.133 % Topical SwabSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130738743120180GTIN-13: 0738743120180
EAN-13: 0738743120180
GTIN-12: 738743120180
UPC-A: 738743120180
GTIN storage (14 digits): 00738743120180
12-018 (002).jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0924-7112-00BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-01BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-01BZK Towelette10 in 1 CARTONSWAB101
0924-7112-02BZK Towelette10 in 1 CARTONSWAB101
0924-7112-02BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-03BZK Towelette25 in 1 CARTONSWAB251
0924-7112-03BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-04BZK Towelette50 in 1 CARTONSWAB501
0924-7112-04BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-05BZK Towelette1.4 mL in 1 POUCHSWAB1.41
0924-7112-05BZK Towelette100 in 1 CARTONSWAB1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0924-7112BZK TOWELETTE (BENZALKONIUM CHLORIDE) SWAB [ACME UNITED CORPORATION]1Current NDC, Legacy NDC, 11 package rows20190416_866fdc1e-19b2-4d79-e053-2a91aa0a36fe.zip

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
0924-71120924-7112-00, 0924-7112-01, 0924-7112-02, 0924-7112-03, 0924-7112-04, 0924-7112-05
65517-0004

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
BZK ToweletteBENZALKONIUM CHLORIDEAcme United Corporation866fdc1e-19b2-4d79-e053-2a91aa0a36fe2019-04-16WarningsExact identifier
ndc (package): 0924-7112-04
ndc (package): 0924-7112-02
ndc (package): 0924-7112-03
ndc (package): 0924-7112-00
ndc (package): 0924-7112-01
ndc (package): 0924-7112-05
ndc (product): 0924-7112
ndc11 (package): 00924711202
ndc11 (package): 00924711205
ndc11 (package): 00924711201
ndc11 (package): 00924711203
ndc11 (package): 00924711204
ndc11 (package): 00924711200
spl id: 866f9e78-87a0-7919-e053-2a91aa0a4058
spl set id: 866fdc1e-19b2-4d79-e053-2a91aa0a36fe

Reported adverse events (FAERS/openFDA)#

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