Home NDC 48951-8443 Sarothamnus Aurum
Product NDC 48951-8443
11-digit product format 489518443
Labeler code 48951
Product ID 48951-8443_5723a03e-4c23-0d69-e063-6294a90a38df
Type HUMAN OTC DRUG
Nonproprietary name Sarothamnus Aurum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance CYTISUS SCOPARIUS FLOWER; SELENICEREUS GRANDIFLORUS STEM; CAMPHOR (NATURAL); GOLD
Active strength 3; 4; 4; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sarothamnus Aurum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CYTISUS SCOPARIUS FLOWER 3 [hp_X]/mL SELENICEREUS GRANDIFLORUS STEM 4 [hp_X]/mL CAMPHOR (NATURAL) 4 [hp_X]/mL GOLD 15 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Socrata Ingredients# 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 48951-8443-1 48951844301 10 AMPULE in 1 BOX (48951-8443-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current