Fusion Antibacterial Wipes

Manufacturer
Fusion Products Ltd. | Hangzhou Lookon Commodity Co., Ltd.
Effective date
2021-06-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:41:07

Label at a glance#

ProductFusion Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Apply to clean dry hands. Wet hands thoroughly with the product and allow to dry Children under 6 should be supervised when using this product

Storage and handling

Do not store above 104°F (40°C) Do not use if seal is missing or broken

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to clean dry hands.

Wet hands thoroughly with the product and allow to dry

Children under 6 should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

Do not store above 104°F (40°C)

Do not use if seal is missing or broken

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, decyl glucoside, glycerin, water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70 WIPES, NDC: 80336-004-09

70 in bottle label70 in bottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80336-004-092023-01-30C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes
80336-004-092022-08-23C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes
80336-004-092022-07-29C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80336-004-09Fusion Antibacterial Wipes70 in 1 BOTTLECLOTH704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80336-004FUSION ANTIBACTERIAL WIPES (ANTIBACTERIAL WET WIPES) CLOTH [FUSION PRODUCTS LTD.]4Legacy NDC, 1 package rows20210630_b2c53fa7-a74f-8fc1-e053-2a95a90a8942.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
80336-00480336-004-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
c5f2f7cc-662a-2a4d-e053-2995a90ad87cb2c53fa7-a74f-8fc1-e053-2a95a90a89422021-06-29WarningsExact identifier
spl id: c5f2f7cc-662a-2a4d-e053-2995a90ad87c
spl set id: b2c53fa7-a74f-8fc1-e053-2a95a90a8942

Reported adverse events (FAERS/openFDA)#

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