Podocon 25
Podocon-25® (25% podophyllin in benzoin tincture)
Approved
Approval ID
a13345b7-c42b-4459-b0ff-03cf91e46b7d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 17, 2023
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Podophyllum resin
PRODUCT DETAILS
NDC Product Code63629-8699
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateFebruary 23, 2022
Generic NamePodophyllum resin
INGREDIENTS (3)
PODOPHYLLUM RESINActive
Quantity: 1 mg in 4 mL
Code: 16902YVY2B
Classification: ACTIB
STYRAX BENZOIN RESINInactive
Code: FE663Z8IRO
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT