JUC Sterilization Wipes

Manufacturer
NMS Technologies Co., Ltd. | A03 Lab of BTS
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:28:28

Label at a glance#

ProductJUC Sterilization Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Unpack and unfold the wipes. From one side of the skin or surface of the object, wipe orderly to cover the entire surface.

Storage and handling

Storage: Avoids light, sealed and stored in a cool place.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 3mg/mL. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial.

When using

OTC - WHEN USING SECTION

avoid direct contact with eyes and damaged skin.

Do not use

OTC - DO NOT USE SECTION

Do not replace wipes used for medical procedures.

Stop use

OTC - STOP USE SECTION

Stop use if there is discomfort, please immediately seek medical attention.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

This product should be placed out of reach of children.

Indications & usage

INDICATIONS & USAGE SECTION

This product can be directly wiped to form a physical antimicrobial film to kill Escherichia coli, Staphylococcus aureus.

Directions

DOSAGE & ADMINISTRATION SECTION

Unpack and unfold the wipes. From one side of the skin or surface of the object, wipe orderly to cover the entire surface.

Warnings

WARNINGS SECTION

This product avoids direct contact with eyes and damaged skin.

Other information

STORAGE AND HANDLING SECTION

Storage: Avoids light, sealed and stored in a cool place.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water.

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

W080W080

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
78128-10178128-101-27

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
299b7b5a-a821-e851-e063-6294a90a3990a6a274d1-1245-22e6-e053-2995a90ae62f2024-12-19WarningsExact identifier
spl set id: a6a274d1-1245-22e6-e053-2995a90ae62f

Reported adverse events (FAERS/openFDA)#

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