Benzethonium Chloride and Dyclonine Hydrochloride

Manufacturer
Rite Aid Corporation
Effective date
2025-06-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:36:41

Label at a glance#

ProductBenzethonium Chloride and Dyclonine Hydrochloride
Active ingredientBENZETHONIUM CHLORIDE, DYCLONINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

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

Dosage and administration

for adults and children 2 years of age or older clean affected area apply a smalll 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 ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium chloride 0.2%

Dyclonine hydrochoride 0.75%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

  • first aid to prevent bacterial contamination in minor cuts, scrapes and burns
  • for 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

  • condition persists or gets worse
  • symptoms persists for more than 7 days or clear up and occur again within a few days
  • 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

  • for adults and children 2 years of age or older
  • clean affected area
  • apply a smalll 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° to 25°C (68° to 77°F)
  • 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 alcohol 40

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rite Aid

LIQUID BANDAGE

TOPICAL ANALGESIC & ANTISEPTIC

For small cuts & wounds

To help prevent infection

Antiseptic formula dries to form an invisible protective cover that is flexible

NET 1.0 FL OZ (29.6 mL)

Use Liquid Bandage for blisters, chapped & cracked fingertips, hangnails, paper cuts, shaving nicks, & help in preventing the formulation of calluses

Great for: athletes, active lifestyles, outdoor sportsmen & musicians

Liquid BandageLiquid Bandage

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-0779-32024-02-12C16284748780-1f386c64a-2932-0266-e053-dadaa90a7c1aLiquid Bandage 1 fl oz (30 mL)
11822-0779-32023-01-30C16284748780-1f386c64a-2932-0266-e053-dadaa90a7c1aLiquid Bandage 1 fl oz (30 mL)

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
11822-077911822-0779-3

Ingredients#

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

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

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
38101cef-7e18-c0b5-e063-6394a90a0774ae42b754-9a06-6e80-e053-2a95a90a740d2025-06-21WarningsExact identifier
spl id: 38101cef-7e18-c0b5-e063-6394a90a0774
spl set id: ae42b754-9a06-6e80-e053-2a95a90a740d

Reported adverse events (FAERS/openFDA)#

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