Podocon 25

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7133529251
1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR

Annotations

UNII (FDA Substance ID)

16902YVY2B

PODOPHYLLUM RESIN

RxCUI 8462

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "16902YVY2B",
    "rxcui": "8462",
    "inchikey": null,
    "display_name": "PODOPHYLLUM RESIN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "790711b3-2168-4a19-b5c9-e46bf06143f6": {
      "match": "brand_token",
      "title": "PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [BRYANT RANCH PREPACK]",
      "spl_version": "100",
      "published_date": "2025-11-17"
    }
  },
  "productid": "71335-2925_c4e909ba-10b5-4c09-afea-4c5d151f657a",
  "productndc": "71335-2925",
  "dosage_form": "TINCTURE",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PODOPHYLLUM RESIN",
  "proprietary_name": "Podocon 25",
  "active_ingred_unit": "mg/4mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Podophyllum resin",
  "start_marketing_date": "19900901",
  "active_numerator_strength": "1"
}

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