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Benzethonium Chloride and Dyclonine Hydrochloride

Liquid Bandage 1 fl oz (30 mL)

Approved
Approval ID

ae42b754-9a06-6e80-e053-2a95a90a740d

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Jun 21, 2025

Manufacturers
FDA

Rite Aid Corporation

DUNS: 014578892

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Liquid Bandage

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code11822-0779
Application NumberM003
Product Classification
M
Marketing Category
C200263
G
Generic Name
Liquid Bandage
Product Specifications
Route of AdministrationTOPICAL
Effective DateJune 21, 2025
FDA Product Classification

INGREDIENTS (8)

BENZETHONIUM CHLORIDEActive
Quantity: 0.2 mg in 30 mL
Code: PH41D05744
Classification: ACTIB
PYROXYLINInactive
Code: KYR8BR2X6O
Classification: IACT
ETHYL ACETATEInactive
Code: 76845O8NMZ
Classification: IACT
DYCLONINE HYDROCHLORIDEActive
Quantity: 0.75 mg in 30 mL
Code: ZEC193879Q
Classification: ACTIB
ACETONEInactive
Code: 1364PS73AF
Classification: IACT
AMYL ACETATEInactive
Code: 92Q24NH7AS
Classification: IACT
CASTOR OILInactive
Code: D5340Y2I9G
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 9/1/2020

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 Bandage

INDICATIONS & USAGE SECTION

LOINC: 34067-9Updated: 9/1/2020

Uses

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

OTC - ACTIVE INGREDIENT SECTION

LOINC: 55106-9Updated: 9/1/2020

Active ingredient

Benzethonium chloride 0.2%

Dyclonine hydrochoride 0.75%

OTC - PURPOSE SECTION

LOINC: 55105-1Updated: 9/1/2020

Purpose

First aid antiseptic

Topical analgesic

WARNINGS SECTION

LOINC: 34071-1Updated: 9/1/2020

Warnings

For external use only.

Flammable:

Keep away from fire or flame.

Do not use

  • 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

  • deep or puncture wounds
  • deep cuts
  • animal bites
  • serious burns

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • 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.

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

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 9/1/2020

Directions

  • 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 SAFETY INFORMATION

LOINC: 60561-8Updated: 9/1/2020

Other 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 INGREDIENT SECTION

LOINC: 51727-6Updated: 9/1/2020

Inactive ingredients

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

OTC - QUESTIONS SECTION

LOINC: 53413-1Updated: 9/1/2020

Questions?

Call 1-866-964-0939

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Benzethonium Chloride and Dyclonine Hydrochloride - FDA Drug Approval Details