BRYONIA ALB

UNIISPL

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

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
1563126380
10 mL in 1 BOTTLE (15631-2638-0)
ndc11
1563126381
30 mL in 1 BOTTLE (15631-2638-1)

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": "15631-2638_19ba2026-e106-d690-e063-6394a90a5501",
  "productndc": "15631-2638",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BRYONIA ALBA ROOT",
  "proprietary_name": "BRYONIA ALB",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BRYONIA ALB",
  "start_marketing_date": "20240523",
  "active_numerator_strength": "3"
}

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