Benzethonium chloride and Dyclonine hydrochloride
Quality Choice Liquid Bandage
Approved
Approval ID
34062b23-52aa-99ae-e063-6294a90ae73f
Product Type
HUMAN OTC DRUG LABEL
Effective Date
May 1, 2025
Manufacturers
FDA
Chain Drug Marketing Association
DUNS: 011920774
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 Code83324-232
Application NumberM003
Product Classification
M
Marketing Category
C200263
G
Generic Name
Liquid Bandage
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 1, 2025
FDA Product Classification
INGREDIENTS (8)
ACETONEInactive
Code: 1364PS73AF
Classification: IACT
AMYL ACETATEInactive
Code: 92Q24NH7AS
Classification: IACT
CASTOR OILInactive
Code: D5340Y2I9G
Classification: IACT
ETHYL ACETATEInactive
Code: 76845O8NMZ
Classification: IACT
PYROXYLINInactive
Code: KYR8BR2X6O
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
BENZETHONIUM CHLORIDEActive
Quantity: 2 mg in 1 mL
Code: PH41D05744
Classification: ACTIB
DYCLONINE HYDROCHLORIDEActive
Quantity: 7.5 mg in 1 mL
Code: ZEC193879Q
Classification: ACTIB