BZK Antiseptic Towelette

Manufacturer
Davemed Healthcare Co., Ltd
Effective date
2019-01-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:19

Label at a glance#

ProductBZK Antiseptic Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Tear at notch Remove towelette Use only once As a first aid antiseptic clean affected area apply 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

First aid antiseptic to help prevent skin infection in

  • minor cuts
  • scrapes, burns, anitiseptic cleansing
  • perineal and maternity care

Warnings

WARNINGS SECTION

For external use only

Do not use:

  • as an antiseptic for more than 1 week
  • in the eyes
  • over large areas of the body

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use

  • if irritation and redness develop
  • if condition persists more than 72 hours, consult a physician

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.if swallowed get medical help or contact Poison control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear at notch
  • Remove towelette
  • Use only once

As a first aid antiseptic

  • clean affected area
  • apply 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

OTHER SAFETY INFORMATION

  • Store at room temperature
  • Avoid excessive heat

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
70897-005-012024-01-30C16284748780-11030e365-21ea-111a-e063-dadaa90a10e2BZK Antiseptic Towelette

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70897-005-01BZK Antiseptic Towelette1 in 1 POUCHSWAB11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70897-005BZK ANTISEPTIC TOWELETTE (BENZALKONIUM CHLORIDE) SWAB [DAVEMED HEALTHCARE CO., LTD]1Legacy NDC, 1 package rows20190125_8039dbf4-4fdf-f5a6-e053-2991aa0ab210.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
70897-00570897-005-01

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
8039dbf4-4fe0-f5a6-e053-2991aa0ab2108039dbf4-4fdf-f5a6-e053-2991aa0ab2102019-01-24WarningsExact identifier
spl id: 8039dbf4-4fe0-f5a6-e053-2991aa0ab210
spl set id: 8039dbf4-4fdf-f5a6-e053-2991aa0ab210

Reported adverse events (FAERS/openFDA)#

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