Pulmo Mercurius

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
4895180891
10 AMPULE in 1 BOX (48951-8089-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

FXS1BY2PGL

MERCURY

RxCUI 6769

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "FXS1BY2PGL",
    "rxcui": "6769",
    "inchikey": "QSHDDOUJBYECFT-UHFFFAOYSA-N",
    "display_name": "MERCURY",
    "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": "48951-8089_49efbceb-17ae-fdfb-e063-6294a90ac155",
  "productndc": "48951-8089",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MERCURY; SUS SCROFA LUNG",
  "proprietary_name": "Pulmo Mercurius",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulmo Mercurius",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "17; 8"
}

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