Antiseptic Bandages

Manufacturer
Pharmaband
Effective date
2014-09-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:40:31

Label at a glance#

ProductAntiseptic Bandages
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

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

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#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

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

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 Ingredients: 

INACTIVE INGREDIENT SECTION

None

Other Information: 

OTHER SAFETY INFORMATION

Not intended for use on delicate or sensitive skin.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PharmaBand
Antiseptic Bandages

20

Antiseptic

Bandages

PRINCIPAL DISPLAY PANEL PharmaBand Antiseptic Bandages 20 Antiseptic BandagesPRINCIPAL DISPLAY PANEL PharmaBand Antiseptic Bandages 20 Antiseptic Bandages

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69225-1000-22020-01-31C16284748780-19d75b9d0-0da8-f424-e053-dadaa90a57ceAntiseptic Bandages
69225-1000-32020-01-31C16284748780-19d75b9d0-0da8-f424-e053-dadaa90a57ceAntiseptic Bandages
69225-1000-42020-01-31C16284748780-19d75b9d0-0da8-f424-e053-dadaa90a57ceAntiseptic Bandages

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69225-1000-2Antiseptic Bandages20 in 1 BOXDRESSING203
69225-1000-3Antiseptic Bandages30 in 1 BOXDRESSING303
69225-1000-4Antiseptic Bandages40 in 1 BOXDRESSING403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69225-1000ANTISEPTIC BANDAGES (BENZALKONIUM CHLORIDE) DRESSING [PHARMABAND]3Legacy NDC, 3 package rows20141015_b5a44e5f-c84a-40e2-831b-08925d7ef97e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W73
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y3

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69225-100069225-1000-2, 69225-1000-3, 69225-1000-4

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
NATURAL LATEX RUBBER2LQ0UUW8INCNTM

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
e50d75d0-b3e6-41d3-b335-969c9d0c7907b5a44e5f-c84a-40e2-831b-08925d7ef97e2014-09-22WarningsExact identifier
spl id: e50d75d0-b3e6-41d3-b335-969c9d0c7907
spl set id: b5a44e5f-c84a-40e2-831b-08925d7ef97e

Reported adverse events (FAERS/openFDA)#

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