coralite ANTIBACTERIAL BANDAGES

Manufacturer
YIWU HAODING MEDICAL CO.,LTD
Effective date
2023-03-03
Label type
HUMAN OTC DRUG LABEL
Version
72
Source
full-release
Hydrated at
2026-05-31 23:54:23

Label at a glance#

Productcoralite ANTIBACTERIAL BANDAGES
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 condition persists or gets worse.

Do not use longer than 1 week unless directed by a physician. In case of deep or puncture wounds, animal bites, or serious burn, consult a physician.

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

image description
image description

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69139-106-01coralite ANTIBACTERIAL BANDAGES30 in 1 BOXSWAB3072
69139-106-01coralite ANTIBACTERIAL BANDAGES0.5 g in 1 POUCHSWAB0.572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69139-106CORALITE ANTIBACTERIAL BANDAGES (BENZALKONIUM CHLORIDE) SWAB [YIWU HAODING MEDICAL CO.,LTD]72Legacy NDC, 2 package rows20230307_d79c4388-17c2-4e26-8ffa-9df497a0af97.zip

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
69139-10669139-106-01

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
f60c4312-ccb9-3e9c-e053-2995a90a2524d79c4388-17c2-4e26-8ffa-9df497a0af972023-03-03WarningsExact identifier
spl id: f60c4312-ccb9-3e9c-e053-2995a90a2524
spl set id: d79c4388-17c2-4e26-8ffa-9df497a0af97

Reported adverse events (FAERS/openFDA)#

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