Home NDC 71335-2925 Podocon 25
Product NDC 71335-2925
11-digit product format 713352925
Labeler code 71335
Product ID 71335-2925_c4e909ba-10b5-4c09-afea-4c5d151f657a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Podophyllum resin
Dosage form TINCTURE
Route TOPICAL
Labeler Bryant Ranch Prepack
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1990-09-01
Substance PODOPHYLLUM RESIN
Active strength 1 mg/4mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Podocon 25
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PODOPHYLLUM RESIN 1 mg/4mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 16902YVY2B Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71335-2925-1 Podocon 25 15 mL in 1 BOTTLE, WITH APPLICATOR TINCTURE 15 100 71335-2925-1 Podocon 25 1 in 1 CARTON TINCTURE 1 100
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 71335-2925-1 71335292501 1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR 2025-10-21 No No Current