Podocon 25

NDC 71335-2925 · Bryant Ranch Prepack

Generic namePodophyllum resin

Dosage formTINCTURE

RouteTOPICAL

Active ingredient(s)PODOPHYLLUM RESIN

Strength1 mg/4mL

Marketing categoryUNAPPROVED DRUG OTHER

Packages

71335-2925-1 — 1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0574-0601 — Podophyllum resin, 43857-0328 — Boldo, Carduus Marianus, Curcuma Longa, Echinacea (Angustifolia), Taraxacum Officinale Magnesia Phosphorica, Gallbladder (Bovine), Hepar Bovine, Ammi Visnaga, Atropinum Sulphuricum, Chelidonium Majus, Leptandra Virginica, Podophyllinum, 63479-1808 — ADENOSINE TRIPHOSPHATE, AMMONIUM MURIATICUM, BAPTISIA TINCTORIA, COLCHICUM AUTUMNALE, JUNIPERUS COMMUNIS, LEVOTHYROXINE, PODOPHYLLINUM, RHUS TOXICODENDRON, 63479-1809 — ADENOSINE TRIPHOSPHATE, BAPTISIA TINCTORIA ROOT, CEANOTHUS AMERICANUS LEAF, FUCUS VESICULOSUS, PODOPHYLLUM RESIN, SEPIA OFFICINALIS JUICE, TESTOSTERONE, 63479-2508 — ADENOSINE TRIPHOSPHATE, AMMONIUM MURIATICUM, BAPTISIA TINCTORIA, COLCHICUM AUTUMNALE, JUNIPERUS COMMUNIS, LEVOTHYROXINE, PODOPHYLLINUM, RHUS TOXICODENDRON, 63479-2509 — ADENOSINE TRIPHOSPHATE, BAPTISIA TINCTORIA ROOT, CEANOTHUS AMERICANUS LEAF, FUCUS VESICULOSUS, PODOPHYLLUM RESIN, SEPIA OFFICINALIS JUICE, TESTOSTERONE, 63629-8699 — Podophyllum resin, 72162-1117 — Podophyllum resin

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.