FDA.reportPublic FDA data

Benzethonium chloride Plus Dyclonine hydrochloride

Manufacturer
VALU MERCHANDISERS, CO
Effective date
2025-11-24
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:17:55

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

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Best Choice

For Small Cuts & Wounds

Liquid Bandage

Antiseptic to Help Prevent Infection

  • Invisible
  • Flexible
  • Waterproof
  • Easy to use

Use liquid bandage for:

blisters, chapped & cracked finger tips, hangnails, paper cuts, shaving nicks & help in preventing the formation of calluses.

Also Used by:

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

0.3 FL OZ (9 mL)

Best Choice_Liquid Bandage_53-033BC.jpgBest Choice_Liquid Bandage_53-033BC.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130000000000000GTIN-13: 0000000000000
EAN-13: 0000000000000
GTIN-12: 000000000000
UPC-A: 000000000000
GTIN storage (14 digits): 00000000000000		Best Choice_Liquid Bandage_53-033BC.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
63941-546-03Benzethonium chloride Plus Dyclonine hydrochloride9 mL in 1 BOTTLE, WITH APPLICATORLIQUID910

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
63941-54663941-546-03

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

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-11-07full-release2026-06-01 00:36:09

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 BANDAGEVALU MERCHANDISERS, COc79540fe-b972-41a4-a215-e21e30b903d12025-11-24WarningsExact identifier
ndc (package): 63941-546-03
ndc (product): 63941-546
ndc11 (package): 63941054603
spl id: 445c0748-5eca-d855-e063-6394a90a94ec
spl set id: c79540fe-b972-41a4-a215-e21e30b903d1

Reported adverse events (FAERS/openFDA)#

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