Home NDC 48951-1281 Aurum Hypericum
Product NDC 48951-1281
11-digit product format 489511281
Labeler code 48951
Product ID 48951-1281_2b60faeb-ae3c-a524-e063-6294a90a4aa2
Type HUMAN OTC DRUG
Nonproprietary name Aurum Hypericum
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance APIS MELLIFERA; GOLD TRICHLORIDE; HYPERICUM PERFORATUM; MAGNESIUM; MAMMAL LIVER; OAT; PHOSPHORIC ACID; SILICON DIOXIDE; STRYCHNOS IGNATII SEED
Active strength 6; 7; 3; 5; 5; 3; 5; 7; 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Aurum Hypericum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OAT 3 [hp_X]/1 HYPERICUM PERFORATUM 3 [hp_X]/1 PHOSPHORIC ACID 5 [hp_X]/1 STRYCHNOS IGNATII SEED 5 [hp_X]/1 MAMMAL LIVER 5 [hp_X]/1 MAGNESIUM 5 [hp_X]/1 APIS MELLIFERA 6 [hp_X]/1 SILICON DIOXIDE 7 [hp_X]/1 GOLD TRICHLORIDE 7 [hp_X]/1
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-1281-2 Aurum Hypericum 1350 in 1 BOTTLE, GLASS PELLET 1350 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1281 AURUM HYPERICUM PELLET [URIEL PHARMACY INC] 6 Current NDC, Legacy NDC, 1 package rows 20250112_be0da1f0-06a1-11df-8a39-0800200c9a66.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 Marketing end Sample Exclude flag Status 48951-1281-2 48951128102 1350 PELLET in 1 BOTTLE, GLASS (48951-1281-2) 1350 pellet 2009-09-01 0000-00-00 No No Current