Home NDC 48951-7000 Magnesite Viscum
Product NDC 48951-7000
11-digit product format 489517000
Labeler code 48951
Product ID 48951-7000_5a96ebfe-6e0f-a284-e063-6294a90aaf1f
Type HUMAN OTC DRUG
Nonproprietary name Magnesite Viscum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance VISCUM ALBUM FRUITING TOP; APIS MELLIFERA; SUS SCROFA UMBILICAL CORD; BOS TAURUS PITUITARY GLAND; BOS TAURUS MAMMARY GLAND; MAGNESITE
Active strength 5; 6; 6; 6; 6; 8 [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], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 48951-7000-1 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 48951-7000-1 f5e01cc5f278…a2eaf40c39c3…
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 Magnesite Viscum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VISCUM ALBUM FRUITING TOP 5 [hp_X]/mL APIS MELLIFERA 6 [hp_X]/mL SUS SCROFA UMBILICAL CORD 6 [hp_X]/mL BOS TAURUS PITUITARY GLAND 6 [hp_X]/mL BOS TAURUS MAMMARY GLAND 6 [hp_X]/mL MAGNESITE 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Socrata Ingredients# 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 48951-7000-1 48951700001 10 AMPULE in 1 BOX (48951-7000-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current