FDA.reportPublic FDA data

BANDAGE

Manufacturer
Dongyang Haodi Medical CO.,Ltd
Effective date
2014-07-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:39:48

Label at a glance#

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride  0.12%

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 dondition 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.

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

None

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69119-001-012019-11-27C16284748780-19855e2a2-46ad-60a7-e053-dbdaa90a05bdf867ffd5-e4ed-4ef0-b8ed-afba53d59b51
69119-001-022019-11-27C16284748780-19855e2a2-46ad-60a7-e053-dbdaa90a05bdf867ffd5-e4ed-4ef0-b8ed-afba53d59b51
69119-001-032019-11-27C16284748780-19855e2a2-46ad-60a7-e053-dbdaa90a05bdf867ffd5-e4ed-4ef0-b8ed-afba53d59b51

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69119-001-01BANDAGE24 in 1 CARTONSWAB242
69119-001-01BANDAGE40 in 1 BOXSWAB402
69119-001-02BANDAGE40 in 1 BOXSWAB402
69119-001-02BANDAGE36 in 1 CARTONSWAB362
69119-001-03BANDAGE12 in 1 CARTONSWAB122
69119-001-03BANDAGE40 in 1 BOXSWAB402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69119-001BANDAGE (BENZALKONIUM CHLORIDE) SWAB [DONGYANG HAODI MEDICAL CO.,LTD ]2Legacy NDC, 6 package rows20140724_f867ffd5-e4ed-4ef0-b8ed-afba53d59b51.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W72
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y2
COTTON FIBERINACTIVE INGREDIENT70LDW53ROO2

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
69119-00169119-001-02, 69119-001-01, 69119-001-03

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
COTTON FIBER70LDW53ROOIACT

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
fc134c19-d4aa-46cb-ac13-07a1e192bb08f867ffd5-e4ed-4ef0-b8ed-afba53d59b512014-07-24WarningsExact identifier
spl id: fc134c19-d4aa-46cb-ac13-07a1e192bb08
spl set id: f867ffd5-e4ed-4ef0-b8ed-afba53d59b51

Reported adverse events (FAERS/openFDA)#

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