Home NDC 48951-2018 Bambusa Stannum
Product NDC 48951-2018
11-digit product format 489512018
Labeler code 48951
Product ID 48951-2018_557ebd9b-5067-89b1-e063-6294a90a7ed1
Type HUMAN OTC DRUG
Nonproprietary name Bambusa Stannum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BAMBUSA VULGARIS WHOLE; STACHYS OFFICINALIS; BOS TAURUS INTERVERTEBRAL DISC; ROSMARINUS OFFICINALIS FLOWERING TOP; FORMICA RUFA; TIN; SILICON DIOXIDE; EQUISETUM ARVENSE TOP
Active strength 6; 6; 6; 6; 7; 7; 12; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 Bambusa Stannum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BAMBUSA VULGARIS WHOLE 6 [hp_X]/mL STACHYS OFFICINALIS 6 [hp_X]/mL BOS TAURUS INTERVERTEBRAL DISC 6 [hp_X]/mL ROSMARINUS OFFICINALIS FLOWERING TOP 6 [hp_X]/mL FORMICA RUFA 7 [hp_X]/mL TIN 7 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL EQUISETUM ARVENSE TOP 15 [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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-2018-1 Bambusa Stannum 10 in 1 PACKAGE LIQUID 10 3 48951-2018-1 Bambusa Stannum 1 mL in 1 AMPULE LIQUID 1 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2018 BAMBUSA STANNUM LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20180518_a0d4d0ac-e2d2-4381-8f93-e41719521859.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 48951-2018-1 48951201801 10 AMPULE in 1 PACKAGE (48951-2018-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current