Label at a glance#

ProductFUSTIN Antibacterial wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Dosage and administration

For use apply thoroughly to hands and skinasdesred. Discard wipe in trash receptacle after use. Do not flush. Keep the package opening securely shut to prevent the wipes from drying out.

Storage and handling

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Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand deaning to decrease bacteria on the skin.May be used on hand, arms and legs.

Warnings

WARNINGS SECTION

·For eJd:ernal use only.When using this prcxl uct keep oot of eyes.In case of contact with eyes,rinse thorough with water.
·Stop use and ask a doctor if irritation or rashoccurs. These may be signs of a serious condition.
·Keep out of reach of crildren.lf swallowed get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

·Keep out of reach of crildren.lf swallowed get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

·For eJd:ernal use only.When using this prcxl uct keep oot of eyes.In case of contact with eyes,rinse thorough with water.
·Stop use and ask a doctor if irritation or rashoccurs. These may be signs of a serious condition.
·Keep out of reach of crildren.lf swallowed get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

/

OTC - STOP USE SECTION

·Stop use and ask a doctor if irritation or rashoccurs. These may be signs of a serious condition.

Directions

DOSAGE & ADMINISTRATION SECTION

For use apply thoroughly to hands and skinasdesred. Discard wipe in trash receptacle after use. Do not flush. Keep the package opening securely shut to prevent the wipes from drying out.

STORAGE AND HANDLING SECTION

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Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Aloe vera extract, Honeysuckle extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

42129-016-01 80P

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42129-016-01	2022-01-28	C162847	48780-1	d6a99b39-79f5-a426-e053-dadaa90af4c2	42129-016 FUSTIN Antibacterial wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
42129-016-01	FUSTIN Antibacterial wipes	80 in 1 BAG	CLOTH	80		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42129-016	FUSTIN ANTIBACTERIAL WIPES CLOTH [FUSTIN(XIAMEN) COMMODITY CO., LTD]	3	Legacy NDC, 1 package rows	20200822_ac949a8e-f876-8c67-e053-2a95a90a9962.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

FUSTIN Antibacterial wipes
ALOE VERA LEAF
LONICERA CAPRIFOLIUM FLOWER
WATER
BENZALKONIUM CHLORIDE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42129-016	42129-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
LONICERA CAPRIFOLIUM FLOWER	5N1WD9784U	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ad61157f-684a-303b-e053-2a95a90af134			ac949a8e-f876-8c67-e053-2a95a90a9962	2020-08-21	Warnings	Exact identifier spl id: ad61157f-684a-303b-e053-2a95a90af134 spl set id: ac949a8e-f876-8c67-e053-2a95a90a9962

Reported adverse events (FAERS/openFDA)#

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