Bryonia Alba

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
6354555301
200 PELLET in 1 VIAL, GLASS (63545-553-01)
ndc11
6354555302
500 PELLET in 1 VIAL, GLASS (63545-553-02)
ndc11
6354555303
3000 PELLET in 1 BOTTLE, GLASS (63545-553-03)
ndc11
6354555304
10000 PELLET in 1 BOTTLE, GLASS (63545-553-04)

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": "63545-553_de47da97-3d03-afad-e053-2995a90aaaa3",
  "productndc": "63545-553",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BRYONIA ALBA ROOT",
  "proprietary_name": "Bryonia Alba",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Bryonia Alba",
  "start_marketing_date": "20220505",
  "active_numerator_strength": "200"
}

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