Podophyllum Peltatum

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766223411
80 PELLET in 1 VIAL, GLASS (37662-2341-1)
ndc11
3766223412
200 PELLET in 1 VIAL, GLASS (37662-2341-2)
ndc11
3766223413
1200 PELLET in 1 BOTTLE, GLASS (37662-2341-3)
ndc11
3766223414
4000 PELLET in 1 BOTTLE, GLASS (37662-2341-4)

Annotations

UNII (FDA Substance ID)

2S713A4VP3

PODOPHYLLUM

RxCUI 324036

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "2S713A4VP3",
    "rxcui": "324036",
    "inchikey": null,
    "display_name": "PODOPHYLLUM",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "dfdc1756-e5d1-4b05-e053-2995a90ab2bd": {
      "match": "brand_token",
      "title": "PODOPHYLLUM PELT KIT REFILL (PODOPHYLLUM) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]",
      "spl_version": "4",
      "published_date": "2025-01-30"
    }
  },
  "productid": "37662-2341_f20c98a8-0bf3-07f4-e053-2a95a90a44ad",
  "productndc": "37662-2341",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PODOPHYLLUM",
  "proprietary_name": "Podophyllum Peltatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Podophyllum Peltatum",
  "start_marketing_date": "20230112",
  "active_numerator_strength": "30"
}

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