Home NDC 48951-2058 Berberis Viscum
Product NDC 48951-2058
11-digit product format 489512058
Labeler code 48951
Product ID 48951-2058_4394ecfe-79e7-45ef-e063-6394a90a1997
Type HUMAN OTC DRUG
Nonproprietary name Berberis Viscum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BERBERIS VULGARIS ROOT BARK; OXALIS ACETOSELLA LEAF; URTICA URENS; VISCUM ALBUM FRUITING TOP; MAGNESIUM SULFATE, UNSPECIFIED; BOS TAURUS OVARY; ALUMINUM OXIDE; BOS TAURUS UTERUS; PENOXSULAM
Active strength 2; 3; 3; 4; 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
Pharmacologic classes Calculi Dissolution Agent [EPC], 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], 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 Berberis Viscum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 2 [hp_X]/mL OXALIS ACETOSELLA LEAF 3 [hp_X]/mL URTICA URENS 3 [hp_X]/mL VISCUM ALBUM FRUITING TOP 4 [hp_X]/mL MAGNESIUM SULFATE, UNSPECIFIED 6 [hp_X]/mL BOS TAURUS OVARY 6 [hp_X]/mL ALUMINUM OXIDE 6 [hp_X]/mL BOS TAURUS UTERUS 6 [hp_X]/mL PENOXSULAM 10 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 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 48951-2058-1 Berberis Viscum 1 mL in 1 AMPULE LIQUID 1 5 48951-2058-1 Berberis Viscum 10 in 1 BOX LIQUID 10 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2058 BERBERIS VISCUM LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250109_30abbbd6-1657-4959-9f07-85ddf45f1119.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 48951-2058-1 48951205801 10 AMPULE in 1 BOX (48951-2058-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current