FDA.reportPublic FDA data

Benzethonium chloride Plus Dyclonine hydrochloride

Manufacturer
HEB
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:38:07

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 and scrapes

Dosage and administration

Clean affected area apply a small amount on the area 1-3 times daily let dry a second coating may be applied for extra protection to remove, apply more Liquid Bandage and quickly wipe off finger nail polish remover may dissolve Liquid Bandage

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 and scrapes

Warnings

WARNINGS SECTION

For external use only.

Flammable:

SAFE HANDLING WARNING SECTION

do not use while smoking or near heat 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
  • on infected areas or wounds that are draining
  • with other first aid products such as lotions and creams
  • over sutures
  • on mucous membranes

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep puncture wounds
  • deep cuts
  • animal bites
  • serious bleeding
  • diabetes
  • poor circulation
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • do not sotre at temperaure above 120 oF

Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • conditions persists or gets worse
  • infection occurs

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

  • Clean affected area
  • apply a small amount on the area 1-3 times daily
  • let dry
  • a second coating may be applied for extra protection
  • to remove, apply more Liquid Bandage and quickly wipe off
  • finger nail polish remover may dissolve Liquid Bandage

Other information

OTHER SAFETY INFORMATION

  • cap bottle tightly
  • store at room temperature away from heat
  • may temporarily sting upon application
  • do not allow to come in contact with floors, countertops, or other finished 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

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB

Topical Analgesic and

Antiseptic to Help Prevent Infection

Liquid Bandage

For Small Cuts and Wounds

Use liquid bandage for blisters, chapped and cracked fingertips, hangnails, paper cuts, shaving nicks and to help in prevent the formation of calluses.

Used by bowlers, dancers, fishermen, golfers, hikers, musicians, runners, and tennis players.

  • Invisible
  • Flexible
  • Waterproof
  • Easy to Use

0.3 FL OZ (9 mL)

HEB_Liquid Bandage_53-033HE-01.jpgHEB_Liquid Bandage_53-033HE-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1da7d10e-498b-41dd-970f-0f5bd7432f39Product name120190228

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-512-03Benzethonium chloride Plus Dyclonine hydrochloride9 mL in 1 BOTTLE, WITH APPLICATORLIQUID98

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
37808-51237808-512-03

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72024-12-11full-release2026-06-01 00:42:25

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
Benzethonium chloride Plus Dyclonine hydrochlorideLIQUID BANDAGEHEB40b71196-a2ac-4a44-8046-c448d066baa22025-10-07WarningsExact identifier
ndc (package): 37808-512-03
ndc (product): 37808-512
ndc11 (package): 37808051203
spl id: 4094cbfe-fb3e-0d58-e063-6394a90a47cc
spl set id: 40b71196-a2ac-4a44-8046-c448d066baa2

Reported adverse events (FAERS/openFDA)#

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