FDA.reportPublic FDA data

Benzethonium chloride Plus Dyclonine hydrochloride

Manufacturer
Geiss Destin & Dunn Inc.
Effective date
2024-12-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:47:21

Label at a glance#

ProductBenzethonium chloride Plus Dyclonine hydrochloride
Active ingredientBENZETHONIUM CHLORIDE, DYCLONINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

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

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 a second coating may be applied for extra protection children under 2 years of age: 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 prevent bacteria contamination in minor cuts, scrapes and burns
  • for the temporary relief of pain

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
  • deep cuts
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • conditions persists or gets worse
  • infection occurs
  • symptoms persist for more 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
  • a second coating may be applied for extra protection
  • children under 2 years of age: consult a doctor

Other information

OTHER SAFETY INFORMATION

  • cap bottle tightly
  • store between 20°C to 25ºC(68º to 77ºF)
  • may temporarily sting upon application
  • to remove, apply more Liquid Bandage and quickly wipe off

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

GOODSENSE

Liquid

Bandage

Topical analgesic and antiseptic seals to protect

For small cuts and wounds

  • Prevents infection
  • Water-resistant
  • Invisible and flexible
  • Built-in applicator brush

Use Liquid Bandage for:

Blisters, chapped and cracked fingertips, hangnails, paper cuts, shaving nicks and help in preventing the formation of calluses.

Great for:

Athletes, active lifestyles, outdoor sportsmen and musicians.

NET 0.3 FL OZ (9 mL)

Liquid Bandage 1Liquid Bandage 1

Liquid Bandage 2Liquid Bandage 2

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
50804-75550804-755-03

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
ACETONE1364PS73AFIACT
AMYL ACETATE92Q24NH7ASIACT
CASTOR OILD5340Y2I9GIACT
ETHYL ACETATE76845O8NMZIACT
PYROXYLINKYR8BR2X6OIACT
ALCOHOL3K9958V90MIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB
DYCLONINE HYDROCHLORIDEZEC193879QACTIB

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
2a979c9c-d13c-7433-e063-6394a90a401ac6b1643a-9ceb-6c53-e053-2a95a90ad5152024-12-31WarningsExact identifier
spl set id: c6b1643a-9ceb-6c53-e053-2a95a90ad515

Reported adverse events (FAERS/openFDA)#

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