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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63629-8699
Product Classification
G
Generic Name
Podophyllum resin
Product Specifications
Route of AdministrationTOPICAL
Effective DateFebruary 23, 2022
FDA Product Classification
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