Bryonia

UNIISPL

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

Identification

ManufacturerEnergique, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4491103821
30 mL in 1 BOTTLE, DROPPER (44911-0382-1)

Annotations

UNII (FDA Substance ID)

T7J046YI2B

BRYONIA ALBA ROOT

RxCUI 1309676

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "T7J046YI2B",
    "rxcui": "1309676",
    "inchikey": null,
    "display_name": "BRYONIA ALBA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9b6a13ea-a18c-445a-90ef-9507f9e19064": {
      "match": "brand_token",
      "title": "BRYONIA STANNUM PELLET [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2026-02-26"
    }
  },
  "productid": "44911-0382_b5dfb385-847a-433b-a413-f8ad47616f8b",
  "productndc": "44911-0382",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BRYONIA ALBA ROOT",
  "proprietary_name": "Bryonia",
  "active_ingred_unit": "[hp_C]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Bryonia (Alba)",
  "start_marketing_date": "20160819",
  "active_numerator_strength": "200"
}

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