BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE- liquid bandage liquid 
AmerisourceBergen Drug Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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GNP Liquid Bandage

Active ingredients

Benzethonium chloride 0.2%

Dyclonine hydrochloride 0.75%

Purpose

First aid antiseptic

Topical analgesic

Uses

Warnings

For external use only.

Flammable:

do not use while smoking or near heat or flame.

Do not use

  • 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

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

When using this product

  • 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

  • conditions persists or gets worse
  • infection occurs

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

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

Questions

Call 1-866-964-0939

Principal Display Panel

Good Neighbor Pharmacy

For small cuts & wounds

Liquid Bandage

Antiseptic to Help Prevent Infection

Use liquid bandage for:

blisters, chapped & cracked fingertips, hangnails, paper cuts, shaving nicks & help in preventing the formulation of calluses.

Used by:

athletes, active lifestyles, outdoor sportsman & musicians

NET 0.3 FL OZ (9 mL)

Liquid Bandage cardLiquid Bandage label

BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE 
liquid bandage liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-525
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.2 mg  in 9 mL
DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE0.75 mg  in 9 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
AMYL ACETATE (UNII: 92Q24NH7AS)  
CASTOR OIL (UNII: D5340Y2I9G)  
ETHYL ACETATE (UNII: 76845O8NMZ)  
PYROXYLIN (UNII: KYR8BR2X6O)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-525-239 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/21/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/21/2017
Labeler - AmerisourceBergen Drug Corporation (007914906)

Revised: 1/2023
Document Id: f28c1222-500d-ab06-e053-2995a90ad004
Set id: 5c82c4db-258e-4647-aec9-1c4520e0468a
Version: 5
Effective Time: 20230118
 
AmerisourceBergen Drug Corporation