MEDULLA OSSIS SUIS

UNIISPL

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

Identification

ManufacturerBOIRON

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220332941
8 [hp_X] in 1 TUBE (0220-3329-41)

Annotations

UNII (FDA Substance ID)

VP2CN2G7Y8

SUS SCROFA BONE MARROW

RxCUI 1311276

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "VP2CN2G7Y8",
    "rxcui": "1311276",
    "inchikey": null,
    "display_name": "SUS SCROFA BONE MARROW",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1b3db054-999d-40a1-b6bb-5fc29c9e098b": {
      "match": "brand_token",
      "title": "MEDULLA ARNICA PELLET [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2024-02-06"
    }
  },
  "productid": "0220-3329_0a1f531e-55e6-7573-e063-6294a90aaa48",
  "productndc": "0220-3329",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SUS SCROFA BONE MARROW",
  "proprietary_name": "MEDULLA OSSIS SUIS",
  "active_ingred_unit": "[hp_X]/8[hp_X]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "SUS SCROFA BONE MARROW",
  "start_marketing_date": "20180108",
  "active_numerator_strength": "8"
}

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