Cocculus Conium

UNIISPL

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

Identification

ManufacturerUriel Pharmacy Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895131092
1350 PELLET in 1 BOTTLE, GLASS (48951-3109-2)

Annotations

UNII (FDA Substance ID)

XTC0D02P6C

AMBERGRIS

RxCUI 1311494

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "XTC0D02P6C",
    "rxcui": "1311494",
    "inchikey": null,
    "display_name": "AMBERGRIS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "852e9d96-bc27-1dd8-e053-2991aa0abba5": {
      "match": "brand_token",
      "title": "COCCULUS INDICUS (ANAMIRTA COCCULUS SEED\t) PELLET [BOIRON]",
      "spl_version": "3",
      "published_date": "2026-05-13"
    }
  },
  "productid": "48951-3109_2b617508-1882-a05a-e063-6294a90a6f18",
  "productndc": "48951-3109",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMBERGRIS; ANAMIRTA COCCULUS WHOLE; CONIUM MACULATUM ROOT; LIQUID PETROLEUM",
  "proprietary_name": "Cocculus Conium",
  "active_ingred_unit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cocculus Conium",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "7; 4; 4; 9"
}

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