BZK ANTIBACTERIAL

Manufacturer
YIWU HAODING MEDICAL CO.,LTD
Effective date
2023-03-03
Label type
HUMAN OTC DRUG LABEL
Version
71
Source
full-release
Hydrated at
2026-05-31 23:54:22

Label at a glance#

ProductBZK ANTIBACTERIAL
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

for adults and childre of 2 years and over use on hands and face to clean and refresh, allow skin to air dry. for childre under 2 years ask a doctor before use. other information: not intended for use of delicate or sensitive skin.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride  0.10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

skin clean and degerming

Warnings

WARNINGS SECTION

for external use only.

flammable, keep away fro fire or flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact Poison control Center right away.

do not use

OTC - DO NOT USE SECTION

  • in large quantities
  • over large areas of the body
  • in eyes

stop use and ask a doctor if conditions worsen or persist

Directions

DOSAGE & ADMINISTRATION SECTION

for adults and childre of 2 years and over use on hands and face to clean and refresh, allow skin to air dry.

for childre under 2 years ask a doctor before use.

other information:

not intended for use of delicate or sensitive skin.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description
image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN71
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD71
1038856benzalkonium chloride 0.1 % Medicated WipesSY71
1038856benzalkonium chloride 0.1 % Topical SwabSY71

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69139-400-01BZK ANTIBACTERIAL1 in 1 PACKAGESWAB171
69139-400-01BZK ANTIBACTERIAL0.8 g in 1 POUCHSWAB0.871

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69139-400BZK ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SWAB [YIWU HAODING MEDICAL CO.,LTD]71Legacy NDC, 2 package rows20230307_d2f2a972-68b5-4c4b-8112-c78a9094e5ee.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
69139-40069139-400-01

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

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
f60c4312-ccae-3e9c-e053-2995a90a2524d2f2a972-68b5-4c4b-8112-c78a9094e5ee2023-03-03WarningsExact identifier
spl id: f60c4312-ccae-3e9c-e053-2995a90a2524
spl set id: d2f2a972-68b5-4c4b-8112-c78a9094e5ee

Reported adverse events (FAERS/openFDA)#

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