FDA.reportPublic FDA data

BZK Antiseptic Swab

Manufacturer
NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | Lights Medical Manufacture Co., Ltd.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:32:40

Label at a glance#

ProductBZK Antiseptic Swab
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Benzalkonium Chloride 0.4%

OTC - PURPOSE SECTION

Purpose: First Aide Antiseptic

INDICATIONS & USAGE SECTION

Uses: For external use. Help prevent infection. Antiseptic cleasing of face, hand, and body withour soap and water.

WARNINGS SECTION

Warnings:

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away. If usual redness, swelling, or other symptoms occur, consult a physician immediately.

DOSAGE & ADMINISTRATION SECTION

Directions: Tear open packet, unfold towelette and use to clease desire skin area. Discard towelette appropriately after single use.

OTHER SAFETY INFORMATION

Do not use in the eyes or over large area of the body.

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Sodium Bicarbonate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038561benzalkonium Cl 0.4 % Medicated PadPSN6
1038561benzalkonium chloride 4 MG/ML Medicated PadSCD6
1038561benzalkonium chloride 0.4 % Medicated ToweletteSY6
1038561benzalkonium chloride 0.4 % Topical SwabSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73288-003-012023-03-01C16284748780-1ba0f9c33-1e4d-a910-e053-dadaa90a0b8573288-003
73288-003-012023-01-30C16284748780-1ba0f9c33-1e4d-a910-e053-dadaa90a0b8573288-003
73288-003-012021-04-28C16284748780-1ba0f9c33-1e4d-a910-e053-dadaa90a0b8573288-003
73288-003-012021-01-29C16284748780-1ba0f9c33-1e4d-a910-e053-dadaa90a0b8573288-003

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73288-003-01BZK Antiseptic Swab2 in 1 PACKAGESOLUTION26
73288-003-01BZK Antiseptic Swab0.85 mL in 1 PACKETSOLUTION0.856

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
73288-00373288-003-01

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
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
BZK Antiseptic SwabBENZALKONIUM CHLORIDENINGBO TIANBO FIRST AID PRODUCT CO., LTD.94043f4e-fe47-4b6f-8354-30697daaed812026-01-12WarningsExact identifier
ndc (package): 73288-003-01
ndc (product): 73288-003
ndc11 (package): 73288000301
spl id: 483a3158-c2a7-9f42-e063-6294a90a1dc4
spl set id: 94043f4e-fe47-4b6f-8354-30697daaed81

Reported adverse events (FAERS/openFDA)#

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