Pulmo Bryonia

Product NDC
48951-8084
11-digit product format
489518084
Labeler code
48951
Product ID
48951-8084_3b540ddb-39ea-80e5-e063-6294a90ad1e3
Type
HUMAN OTC DRUG
Nonproprietary name
Pulmo Bryonia
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; SUS SCROFA LUNG
Active strength
8; 6; 8; 6; 17 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 Bryonia
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BRYONIA ALBA ROOT8 [hp_X]/mL
GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]/mL
ANTIMONY POTASSIUM TARTRATE8 [hp_X]/mL
FERROSOFERRIC PHOSPHATE6 [hp_X]/mL
SUS SCROFA LUNG17 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
T7J046YI2BInternal UNII lookup
639KR60Q1QInternal UNII lookup
DL6OZ476V3Internal UNII lookup
91GQH8I5F7Internal UNII lookup
7GL3G1COB3Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a6752cc7-ff8c-4c34-a0a9-0658a915c8ccAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8084-1Pulmo Bryonia1 mL in 1 AMPULELIQUID14
48951-8084-1Pulmo Bryonia10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANTIMONY POTASSIUM TARTRATEACTIVE INGREDIENTDL6OZ476V3PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2BPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
FERROSOFERRIC PHOSPHATEACTIVE INGREDIENT91GQH8I5F7PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1QPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE INGREDIENT7GL3G1COB3PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT5PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2BPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
FERROSOFERRIC PHOSPHATEACTIVE MOIETY91GQH8I5F7PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1QPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE MOIETY7GL3G1COB3PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPULMO BRYONIA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8084PULMO BRYONIA LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20180525_a6752cc7-ff8c-4c34-a0a9-0658a915c8cc.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 BryoniaPULMO BRYONIAUriel Pharmacy Inc.a6752cc7-ff8c-4c34-a0a9-0658a915c8cc2025-08-01WarningsExact identifier
ndc (product): 48951-8084

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8084-14895180840110 AMPULE in 1 BOX (48951-8084-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent