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United States · US · US:48951-8425_43e5678b-2e4f-6b11-e063-6394a90ab886
Pulmo Mercurius
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUriel Pharmacy Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11489518425360 mL in 1 BOTTLE, DROPPER (48951-8425-3)
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": "48951-8425_43e5678b-2e4f-6b11-e063-6394a90ab886",
"productndc": "48951-8425",
"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"
}Access this data programmatically
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