Home NDC 48951-8425 Pulmo Mercurius
Product NDC 48951-8425
11-digit product format 489518425
Labeler code 48951
Product ID 48951-8425_43e5678b-2e4f-6b11-e063-6394a90ab886
Type HUMAN OTC DRUG
Nonproprietary name Pulmo Mercurius
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance MERCURY; SUS SCROFA LUNG
Active strength 17; 8 [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pulmo Mercurius
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SUS SCROFA LUNG 17 [hp_X]/mL MERCURY 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7GL3G1COB3 Internal UNII lookup FXS1BY2PGL Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8425-3 Pulmo Mercurius 60 mL in 1 BOTTLE, DROPPER LIQUID 60 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8425 PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.] 5 Current NDC, 1 package rows 20250124_2889ec85-faab-21ab-e063-6394a90aaeda.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 48951-8425-3 48951842503 60 mL in 1 BOTTLE, DROPPER (48951-8425-3) 60 ml 2009-09-01 No No Current