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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
DL6OZ476V3ANTIMONY POTASSIUM TARTRATE28300-74-5ANTIMONY POTASSIUM TARTRATE
T7J046YI2BBRYONIA ALBA ROOTBRYONIA ALBA ROOT
91GQH8I5F7FERROSOFERRIC PHOSPHATEFERROSOFERRIC PHOSPHATE
639KR60Q1QGELSEMIUM SEMPERVIRENS ROOTGELSEMIUM SEMPERVIRENS ROOT
7GL3G1COB3SUS SCROFA LUNGSUS SCROFA LUNG

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-8084-14895180840110 AMPULE in 1 BOX (48951-8084-1) / 1 mL in 1 AMPULE10 ampule2009-09-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Pulmo BryoniaUriel Pharmacy Inc.2025-08-01HUMAN OTC DRUG LABEL4