ANTIBACTERIAL WET WIPES

Manufacturer
JUXIN (Jiangsu) New Material Packaging Co., Ltd.
Effective date
2025-01-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:50:41

Label at a glance#

ProductANTIBACTERIAL WET WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Lift tab on front of pack. Pull up wipe from center of pack. Replace cover. When not using, close center flap cover securely to prevent moisture losse. Unfold wipe to wipe down. Let air dry. If area is extremely dirty, clean first with another wipe for best results. Dispose of wipe after each use

Storage and handling

Storage and disposal: Store in original container in areas inaccessible to children. Keep securely closed. Do not reuse or refill this container. Discard empty container in trash or recycle

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to clean and decrease bacteriaand germs

Warnings

WARNINGS SECTION

Keep container tightly sealed, avoid contact with eyes, not for use on broken or sensitive skin, stop use if skin irritation develops, flush eyes immediately if product enters eyes. Keep away from heat and flame. Call a Poison Control Center or doctor for treatment advice.
Have the product container label with you when calling a Poison Control Center or doctor, or going for treatment

Do not use

OTC - DO NOT USE SECTION

Do not use as a diaper wipe or on sensitive skin
Do not use on unpainted wood
Do not use to clean dishes, glassware or utensils

OTC - WHEN USING SECTION

Do not flush. Rinse toys or food with clean water after cleaning.

OTC - STOP USE SECTION

/

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN AND PETS

Directions

DOSAGE & ADMINISTRATION SECTION

Lift tab on front of pack.
Pull up wipe from center of pack. Replace cover. When not using, close center flap cover securely to prevent moisture losse.
Unfold wipe to wipe down. Let air dry.
If area is extremely dirty, clean first with another wipe for best results. Dispose of wipe after each use

Other information

STORAGE AND HANDLING SECTION

Storage and disposal: Store in original container in areas inaccessible to children. Keep securely closed. Do not reuse or refill this container. Discard empty container in trash or recycle

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Propylene glycol, Glycerol,Perfume, Ethylhexylglycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

001001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812737benzalkonium Cl 0.3 % Medicated PadPSN3
1812737benzalkonium chloride 3 MG/ML Medicated PadSCD3
1812737benzalkonium chloride 0.3 % Medicated WipeSY3
1812737benzalkonium chloride 0.3 % Topical ClothSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79805-002-01ANTIBACTERIAL WET WIPES15 in 1 BAGCLOTH153
79805-002-02ANTIBACTERIAL WET WIPES50 in 1 BAGCLOTH503
79805-002-03ANTIBACTERIAL WET WIPES75 in 1 BOTTLECLOTH753

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79805-002ANTIBACTERIAL WET WIPES CLOTH [JUXIN (JIANGSU) NEW MATERIAL PACKAGING CO., LTD.]3Legacy NDC, 3 package rows20250105_ab2aa8ce-8cf1-b8dc-e053-2995a90a212c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79805-00279805-002-01, 79805-002-02, 79805-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
2ad98fa0-7580-9398-e063-6294a90af000ab2aa8ce-8cf1-b8dc-e053-2995a90a212c2025-01-03WarningsExact identifier
spl id: 2ad98fa0-7580-9398-e063-6294a90af000
spl set id: ab2aa8ce-8cf1-b8dc-e053-2995a90a212c

Reported adverse events (FAERS/openFDA)#

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