Home NDC 48951-7216 Magnesium sulf. Bryonia
Product NDC 48951-7216
11-digit product format 489517216
Labeler code 48951
Product ID 48951-7216_3404ba66-c985-6dd0-e063-6294a90a11eb
Type HUMAN OTC DRUG
Nonproprietary name Magnesium sulf. Bryonia
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ARNICA MONTANA; SUS SCROFA UMBILICAL CORD; BRYONIA ALBA ROOT; APIS MELLIFERA; VESPA CRABRO; BOS TAURUS OVARY; VISCUM ALBUM FRUITING TOP; MAGNESIUM SULFATE, UNSPECIFIED; BOS TAURUS PITUITARY GLAND; TIN
Active strength 3; 6; 4; 5; 5; 6; 6; 6; 6; 10 [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
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 Magnesium sulf. Bryonia
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 3 [hp_X]/mL SUS SCROFA UMBILICAL CORD 6 [hp_X]/mL BRYONIA ALBA ROOT 4 [hp_X]/mL APIS MELLIFERA 5 [hp_X]/mL VESPA CRABRO 5 [hp_X]/mL BOS TAURUS OVARY 6 [hp_X]/mL VISCUM ALBUM FRUITING TOP 6 [hp_X]/mL MAGNESIUM SULFATE, UNSPECIFIED 6 [hp_X]/mL BOS TAURUS PITUITARY GLAND 6 [hp_X]/mL TIN 10 [hp_X]/mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-7216-1 Magnesium sulf. Bryonia 10 in 1 BOX LIQUID 10 3 48951-7216-1 Magnesium sulf. Bryonia 1 mL in 1 AMPULE LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-7216 MAGNESIUM SULF. BRYONIA LIQUID [URIEL PHARMACY INC.] 3 Current NDC, 2 package rows 20250502_9418bb05-afd1-fc80-e053-2a95a90a33a2.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 48951-7216-1 48951721601 10 AMPULE in 1 BOX (48951-7216-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current