Home NDC 48951-2014 Bambusa Pulsatilla
Product NDC 48951-2014
11-digit product format 489512014
Labeler code 48951
Product ID 48951-2014_4484ffa9-1c86-0a1c-e063-6294a90abb65
Type HUMAN OTC DRUG
Nonproprietary name Bambusa Pulsatilla
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BAMBUSA VULGARIS WHOLE; BOS TAURUS INTERVERTEBRAL DISC; EQUISETUM ARVENSE TOP; FERROSOFERRIC PHOSPHATE; FORMICA RUFA; PULSATILLA VULGARIS; ROSMARINUS OFFICINALIS FLOWERING TOP; SILICON DIOXIDE; STACHYS OFFICINALIS; TIN; VISCUM ALBUM FRUITING TOP
Active strength 6; 6; 5; 7; 5; 5; 6; 12; 6; 7; 3 [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; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bambusa Pulsatilla
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VISCUM ALBUM FRUITING TOP 6 [hp_X]/mL EQUISETUM ARVENSE TOP 6 [hp_X]/mL FORMICA RUFA 5 [hp_X]/mL PULSATILLA VULGARIS 7 [hp_X]/mL BAMBUSA VULGARIS WHOLE 5 [hp_X]/mL STACHYS OFFICINALIS 5 [hp_X]/mL BOS TAURUS INTERVERTEBRAL DISC 6 [hp_X]/mL ROSMARINUS OFFICINALIS FLOWERING TOP 12 [hp_X]/mL TIN 6 [hp_X]/mL FERROSOFERRIC PHOSPHATE 7 [hp_X]/mL SILICON DIOXIDE 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 48951-2014-1 Bambusa Pulsatilla 10 in 1 BOX LIQUID 10 5 48951-2014-1 Bambusa Pulsatilla 1 mL in 1 AMPULE LIQUID 1 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2014 BAMBUSA PULSATILLA LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20241121_0776c3be-088d-422c-9c12-08fcaae823e1.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 48951-2014-1 48951201401 10 AMPULE in 1 BOX (48951-2014-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current