Home NDC 48951-3264 Cerebellum Thalamus B Aurum
Product NDC 48951-3264
11-digit product format 489513264
Labeler code 48951
Product ID 48951-3264_2c915dcf-001a-9374-e063-6394a90a1580
Type HUMAN OTC DRUG
Nonproprietary name Cerebellum Thalamus B Aurum
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance MYRRH; FRANKINCENSE; BOS TAURUS CEREBELLUM; BOS TAURUS BRAIN; BOS TAURUS PINEAL GLAND; BOS TAURUS NERVE; BIFENTHRIN; SUS SCROFA THALAMUS; GOLD; SUS SCROFA EAR
Active strength 7; 7; 8; 8; 8; 8; 8; 8; 10; 17 [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; [hp_X]/1
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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 Cerebellum Thalamus B Aurum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MYRRH 7 [hp_X]/1 FRANKINCENSE 7 [hp_X]/1 BOS TAURUS CEREBELLUM 8 [hp_X]/1 BOS TAURUS BRAIN 8 [hp_X]/1 BOS TAURUS PINEAL GLAND 8 [hp_X]/1 BOS TAURUS NERVE 8 [hp_X]/1 BIFENTHRIN 8 [hp_X]/1 SUS SCROFA THALAMUS 8 [hp_X]/1 GOLD 10 [hp_X]/1 SUS SCROFA EAR 17 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 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 48951-3264-2 Cerebellum Thalamus B Aurum 1350 in 1 BOTTLE, GLASS PELLET 1350 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3264 CEREBELLUM THALAMUS B AURUM PELLET [URIEL PHARMACY INC.] 2 Current NDC, 1 package rows 20250127_11e638f3-feb5-579d-e063-6394a90a5d56.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 48951-3264-2 48951326402 1350 PELLET in 1 BOTTLE, GLASS (48951-3264-2) 1350 pellet 2009-09-01 No No Current