Home NDC 48951-2161 Berberis Oxalis
Product NDC 48951-2161
11-digit product format 489512161
Labeler code 48951
Product ID 48951-2161_557f0c46-6285-e9a7-e063-6294a90aade5
Type HUMAN OTC DRUG
Nonproprietary name Berberis Oxalis
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BERBERIS VULGARIS ROOT BARK; OXALIS STRICTA WHOLE; SAW PALMETTO; URTICA URENS; VISCUM ALBUM FRUITING TOP; MAGNESIUM SULFATE, UNSPECIFIED FORM; BOS TAURUS PROSTATE GLAND; PENOXSULAM; FERRIC PICRATE
Active strength 2; 3; 3; 3; 4; 6; 8; 10; 8 [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], Iron [CS], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 Berberis Oxalis
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 2 [hp_X]/mL OXALIS STRICTA WHOLE 3 [hp_X]/mL SAW PALMETTO 3 [hp_X]/mL URTICA URENS 3 [hp_X]/mL VISCUM ALBUM FRUITING TOP 4 [hp_X]/mL MAGNESIUM SULFATE, UNSPECIFIED FORM 6 [hp_X]/mL BOS TAURUS PROSTATE GLAND 8 [hp_X]/mL PENOXSULAM 10 [hp_X]/mL FERRIC PICRATE 8 [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 48951-2161-1 Berberis Oxalis 1 mL in 1 AMPULE LIQUID 1 5 48951-2161-1 Berberis Oxalis 10 in 1 BOX LIQUID 10 5
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 Sample Exclude flag Status 48951-2161-1 48951216101 10 AMPULE in 1 BOX (48951-2161-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current