FDA.reportPublic FDA data

MK BZK Swab Non-Sterile

Manufacturer
Changzhou Maokang Medical Products Co., Ltd
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:21:12

Label at a glance#

ProductMK BZK Swab Non-Sterile
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Clean the affected area

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

First Aid to help reduce the risk of infection in minor cuts, scrapes and burns.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in the eyes or over large areas of the body

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds or serious burns.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets worse

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

Clean the affected area

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Bicarbonate, Purified Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Updated LabelUpdated Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59050-434-202023-02-03C16284748780-1f386c649-f5df-0266-e053-dadaa90a7c1aMK BZK Swab Non-Sterile
59050-434-202023-01-30C16284748780-1f386c649-f5df-0266-e053-dadaa90a7c1aMK BZK Swab Non-Sterile

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59050-43459050-434-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM BICARBONATE8MDF5V39QOIACT
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
2511c85b-ab68-8970-e063-6394a90a7b9dd6fe6337-c126-437b-9382-7e7f583920c32024-10-22WarningsExact identifier
spl set id: d6fe6337-c126-437b-9382-7e7f583920c3

Reported adverse events (FAERS/openFDA)#

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