Home NDC 48951-2009-2 Bambusa Aurum
Product NDC 48951-2009
Requested package NDC 48951-2009-2
11-digit product format 489512009
Labeler code 48951
Product ID 48951-2009_38954153-3a4d-08a2-e063-6394a90a2eea
Type HUMAN OTC DRUG
Nonproprietary name Bambusa Aurum
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance FORMICA RUFA; BAMBUSA VULGARIS WHOLE; STACHYS OFFICINALIS; BOS TAURUS INTERVERTEBRAL DISC; ROSMARINUS OFFICINALIS FLOWERING TOP; SILICON DIOXIDE; GOLD; ARNICA MONTANA
Active strength 5; 6; 6; 6; 6; 12; 16; 20 [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 Bambusa Aurum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FORMICA RUFA 5 [hp_X]/1 BAMBUSA VULGARIS WHOLE 6 [hp_X]/1 STACHYS OFFICINALIS 6 [hp_X]/1 BOS TAURUS INTERVERTEBRAL DISC 6 [hp_X]/1 ROSMARINUS OFFICINALIS FLOWERING TOP 6 [hp_X]/1 SILICON DIOXIDE 12 [hp_X]/1 GOLD 16 [hp_X]/1 ARNICA MONTANA 20 [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 48951-2009-2 Bambusa Aurum 1350 in 1 BOTTLE, GLASS PELLET 1350 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2009 BAMBUSA AURUM PELLET [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 1 package rows 20180601_43f3dd30-701f-4fa4-9743-d10051c6e6d4.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 48951-2009-2 48951200902 1350 PELLET in 1 BOTTLE, GLASS (48951-2009-2) 1350 pellet 2009-09-01 0000-00-00 No No Current