FDA.reportPublic FDA data

Anti-Bacterial Wipes

Manufacturer
Tongling Jieya Biological Technology Co., Ltd.
Effective date
2025-01-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:50:48

Label at a glance#

ProductAnti-Bacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride  0.155%                        

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses

Antiseptic that kills germs and helps prevent the spread of cold

WARNINGS SECTION

Warnings:

For external use only

May irritate eys. Keep out of  reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

            Directions

  • Lift label to open
  • Remove towel
  • Wipe hands thoroughly. Discard after use.
  • Reseal label to prevent drying

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Propylene Glycol, Aloe Vera, Polysorbate 20, Diazolideinyl Urea, Disodium Cocoamphodiacetate, Fragrance, Tetrasodium EDTA, Citric Acid, Iodopropynyl Buylcarbamate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043322benzalkonium Cl 0.155 % Medicated PadPSN5
1043322benzalkonium chloride 1.55 MG/ML Medicated PadSCD5
1043322benzalkonium chloride 0.155 % Medicated WipeSY5
1043322benzalkonium chloride 0.155 % Topical SwabSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50552-002-01Anti-Bacterial Wipes80 in 1 CANISTERSOLUTION805
50552-002-01Anti-Bacterial Wipes0.5 g in 1 APPLICATORSOLUTION0.55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50552-002ANTI-BACTERIAL WIPES (BENZALKONIUM CHLORIDE) SOLUTION [TONGLING JIEYA BIOLOGICAL TECHNOLOGY CO., LTD.]5Current NDC, Legacy NDC, 2 package rows20250106_d7aeb18f-abf2-49bd-a8a3-ac57f60fbe7d.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50552-00250552-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYSORBATE 207T1F30V5YHIACT
ALOE VERA LEAFZY81Z83H0XIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
EDETATE DISODIUM7FLD91C86KIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
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
Anti-Bacterial WipesBENZALKONIUM CHLORIDETongling Jieya Biological Technology Co., Ltd.d7aeb18f-abf2-49bd-a8a3-ac57f60fbe7d2025-01-04WarningsExact identifier
ndc (package): 50552-002-01
ndc (product): 50552-002
ndc11 (package): 50552000201
spl id: 2aed02d7-1b20-9415-e063-6394a90a4836
spl set id: d7aeb18f-abf2-49bd-a8a3-ac57f60fbe7d

Reported adverse events (FAERS/openFDA)#

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