ANTIBACTERIAL BANDAGE

Manufacturer: International Wholesale, Inc.
Effective date: 2014-09-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:40:17

Label at a glance#

ProductANTIBACTERIAL BANDAGE

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Clean and dry the affected area. Apply a sterile bandage on the area 1 to 3 times daily.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 1 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only.

Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Clean and dry the affected area. Apply a sterile bandage on the area 1 to 3 times daily.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

None

Other information: Not intended for use on delicate or sensitive skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52862-313-30	2019-11-27	C162847	48780-1	9855e2a2-4392-60a7-e053-dbdaa90a05bd	a4a9c51e-47e0-49b6-a1eb-6bdd4b4b8dd1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52862-313-30	ANTIBACTERIAL BANDAGE	0.5 g in 1 POUCH	SWAB	0.5		1
52862-313-30	ANTIBACTERIAL BANDAGE	30 in 1 BOX	SWAB	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52862-313	ANTIBACTERIAL BANDAGE (BENZALKONIUM CHLORIDE) SWAB [INTERNATIONAL WHOLESALE, INC.]	1	Legacy NDC, 2 package rows	20140924_a4a9c51e-47e0-49b6-a1eb-6bdd4b4b8dd1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BENZALKONIUM CHLORIDE	ACTIVE INGREDIENT	F5UM2KM3W7	1
BENZALKONIUM	ACTIVE MOIETY	7N6JUD5X6Y	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

ANTIBACTERIAL BANDAGE
benzalkonium chloride
BENZALKONIUM
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52862-313	52862-313-30

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
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT

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
0dea23f8-c7bc-4cb6-be93-2956036033e2			a4a9c51e-47e0-49b6-a1eb-6bdd4b4b8dd1	2014-09-23	Warnings	Exact identifier spl id: 0dea23f8-c7bc-4cb6-be93-2956036033e2 spl set id: a4a9c51e-47e0-49b6-a1eb-6bdd4b4b8dd1

Reported adverse events (FAERS/openFDA)#

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