FDA.reportPublic FDA data

Liquid Bandage

Manufacturer
Premier Brands of America Inc.
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:38:02

Label at a glance#

ProductLiquid Bandage
Active ingredientBENZETHONIUM CHLORIDE, DYCLONINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

first aid to help prevent infection in minor cuts, scrapes, and burns first aid for the temporary relief of pain in minor cuts, scrapes, and burns

Dosage and administration

for adults and children 2 years of age and older clean affected area apply a small amount on the area 1 to 3 times daily and let dry may be covered with a sterile bandage if bandaged, let dry first children under under 2 years of age; do not sure, consult a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzethonium chloride 0.2%

Dyclonine hydrochloride 0.75%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

  • first aid to help prevent infection in minor cuts, scrapes, and burns
  • first aid for the temporary relief of pain in minor cuts, scrapes, and burns

Warnings

WARNINGS SECTION

For external use only.

Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • in the eyes
  • over large areas of the body
  • longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • conditions persists or gets worse
  • infection occurs
  • symptoms persist for than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • for adults and children 2 years of age and older
  • clean affected area
  • apply a small amount on the area 1 to 3 times daily and let dry
  • may be covered with a sterile bandage
  • if bandaged, let dry first
  • children under under 2 years of age; do not sure, consult a doctor

Other information

OTHER SAFETY INFORMATION

  • cap bottle tightly
  • store between 20° to 25°C (68° to 77°F)
  • may temporarily sting upon application
  • to remove, apply more Liquid Bandage and quickly wipe off
  • do not allow to come into contact with fabrics, floors, countertops or other surfaces - will stain

Inactive ingredients

INACTIVE INGREDIENT SECTION

acetone, amyl acetate, castor oil, ethyl acetate, nitrocellulose, SD slcohol 40

Questions

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KILLS 99.9% OF GERMS

TO HELP PREVENT INFECTION

EndZone

LIQUID

BANDAGE

FOR SMALL CUTS & WOUNDS

BENZETHONIUM CHLORIDE 0.2%/FIRST AID ANTISEPTIC

DYCLONINE HYDROCHLORIDE 0.75%/TOPICAL ANALGESIC

SEALS TO PROTECT

Helps Prevent Infection

Water-Resistant, Invisible & Flexible

1.0 FL OZ (29.6 mL)

Image 1Image 1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1da7d10e-498b-41dd-970f-0f5bd7432f39Product name120190228
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56104-502-00Liquid Bandage29.6 mL in 1 BOTTLE, WITH APPLICATORLIQUID29.65
56104-502-00Liquid Bandage1 in 1 CARTONLIQUID15

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56104-50256104-502-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMYL ACETATE92Q24NH7ASIACT
CASTOR OILD5340Y2I9GIACT
ETHYL ACETATE76845O8NMZIACT
PYROXYLINKYR8BR2X6OIACT
ALCOHOL3K9958V90MIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB
DYCLONINE HYDROCHLORIDEZEC193879QACTIB
ACETONE1364PS73AFIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-14full-release2026-06-01 00:25:02

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
Liquid BandageBENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDEPremier Brands of America Inc.051b68f9-5d6c-3cd7-e063-6394a90aeb352025-10-07WarningsExact identifier
ndc (package): 56104-502-00
ndc (product): 56104-502
ndc11 (package): 56104050200
spl id: 4094375b-31ea-3c3a-e063-6294a90ad8f6
spl set id: 051b68f9-5d6c-3cd7-e063-6394a90aeb35

Reported adverse events (FAERS/openFDA)#

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