Betula Argentum

UNIISPLATC D08AL

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

Identification

ManufacturerUriel Pharmacy Inc.

CountryUS (United States)

ATC codeD08AL

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895120631
10 AMPULE in 1 BOX (48951-2063-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

7S82P3R43Z

APIS MELLIFERA

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7S82P3R43Z",
    "rxcui": null,
    "inchikey": null,
    "display_name": "APIS MELLIFERA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7f436fc5-0983-4ce3-9951-e68e395bcab0": {
      "match": "brand_token",
      "title": "BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2025-06-30"
    }
  },
  "productid": "48951-2063_3894ea71-3636-1458-e063-6394a90a08fd",
  "productndc": "48951-2063",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "APIS MELLIFERA; ARNICA MONTANA; BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; FORMICA RUFA; SILVER",
  "proprietary_name": "Betula Argentum",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Betula Argentum",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "3; 17; 3; 3; 7; 8"
}

Related drugs

Other records sharing ATC code D08AL.

Access this data programmatically

Query Betula Argentum and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs