Pulmo Mercurius

Product NDC
48951-8089
11-digit product format
489518089
Labeler code
48951
Product ID
48951-8089_49efbceb-17ae-fdfb-e063-6294a90ac155
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pulmo Mercurius
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUS SCROFA LUNG17 [hp_X]/mL
MERCURY8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7GL3G1COB3Internal UNII lookup
FXS1BY2PGLInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3859880c-6826-497e-80a5-d63262126e10Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8089-1Pulmo Mercurius1 mL in 1 AMPULELIQUID16
48951-8089-1Pulmo Mercurius10 in 1 BOXLIQUID106

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MERCURYACTIVE INGREDIENTFXS1BY2PGLPULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE INGREDIENT7GL3G1COB3PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1
MERCURYACTIVE MOIETYFXS1BY2PGLPULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE MOIETY7GL3G1COB3PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8089PULMO MERCURIUS LIQUID [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 2 package rows20241208_3859880c-6826-497e-80a5-d63262126e10.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pulmo MercuriusPULMO MERCURIUSUriel Pharmacy Inc.3859880c-6826-497e-80a5-d63262126e102026-02-03WarningsExact identifier
ndc (product): 48951-8089

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8089-14895180890110 AMPULE in 1 BOX (48951-8089-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent