Home NDC 48951-2063 Betula Argentum
Product NDC 48951-2063
11-digit product format 489512063
Labeler code 48951
Product ID 48951-2063_3894ea71-3636-1458-e063-6394a90a08fd
Type HUMAN OTC DRUG
Nonproprietary name Betula Argentum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance APIS MELLIFERA; ARNICA MONTANA; BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; FORMICA RUFA; SILVER
Active strength 3; 17; 3; 3; 7; 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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Betula Argentum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA 3 [hp_X]/mL BETULA PUBESCENS BARK 17 [hp_X]/mL BETULA PUBESCENS LEAF 3 [hp_X]/mL FORMICA RUFA 3 [hp_X]/mL SILVER 7 [hp_X]/mL ARNICA MONTANA 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-2063-1 Betula Argentum 10 in 1 BOX LIQUID 10 4 48951-2063-1 Betula Argentum 1 mL in 1 AMPULE LIQUID 1 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2063 BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20180423_7f436fc5-0983-4ce3-9951-e68e395bcab0.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 48951-2063-1 48951206301 10 AMPULE in 1 BOX (48951-2063-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current