Pulmo Bryonia

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
4895180841
10 AMPULE in 1 BOX (48951-8084-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

DL6OZ476V3

ANTIMONY POTASSIUM TARTRATE

RxCUI 981

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "DL6OZ476V3",
    "rxcui": "981",
    "inchikey": "WBTCZEPSIIFINA-MSFWTACDSA-J",
    "display_name": "ANTIMONY POTASSIUM TARTRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3859880c-6826-497e-80a5-d63262126e10": {
      "match": "brand_token",
      "title": "PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "6",
      "published_date": "2026-02-05"
    }
  },
  "productid": "48951-8084_3b540ddb-39ea-80e5-e063-6294a90ad1e3",
  "productndc": "48951-8084",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; SUS SCROFA LUNG",
  "proprietary_name": "Pulmo Bryonia",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulmo Bryonia",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "8; 6; 8; 6; 17"
}

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