Home NDC 48951-1368 Aurum Hypericum
Product NDC 48951-1368
11-digit product format 489511368
Labeler code 48951
Product ID 48951-1368_3cbd7956-f62d-5668-e063-6294a90a3de3
Type HUMAN OTC DRUG
Nonproprietary name Aurum Hypericum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance MAGNESIUM HYDROXIDE; STRYCHNOS IGNATII SEED; ROYAL JELLY; AVENA SATIVA FLOWERING TOP; PHOSPHORIC ACID; SILICON DIOXIDE; GOLD TRICHLORIDE; ST. JOHN'S WORT; MAMMAL LIVER
Active strength 4; 5; 6; 3; 5; 7; 7; 3; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 Aurum Hypericum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM HYDROXIDE 4 [hp_X]/mL STRYCHNOS IGNATII SEED 5 [hp_X]/mL ROYAL JELLY 6 [hp_X]/mL AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL PHOSPHORIC ACID 5 [hp_X]/mL SILICON DIOXIDE 7 [hp_X]/mL GOLD TRICHLORIDE 7 [hp_X]/mL ST. JOHN'S WORT 3 [hp_X]/mL MAMMAL LIVER 4 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-1368-3 Aurum Hypericum 60 mL in 1 BOTTLE, DROPPER LIQUID 60 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1368 AURUM HYPERICUM LIQUID [URIEL PHARMACY INC.] 3 Current NDC, 1 package rows 20231216_0c3ed6fe-8dce-0496-e063-6394a90add56.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 48951-1368-3 48951136803 60 mL in 1 BOTTLE, DROPPER (48951-1368-3) 60 ml 2009-09-01 No No Current