Home NDC 48951-8125 Renes Betula
Product NDC 48951-8125
11-digit product format 489518125
Labeler code 48951
Product ID 48951-8125_53eccc8d-5910-3869-e063-6294a90ac2d1
Type HUMAN OTC DRUG
Nonproprietary name Renes Betula
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ELYMUS REPENS ROOT; ONONIS REPENS ROOT; PARSLEY; CAPSELLA BURSA-PASTORIS; ARCTOSTAPHYLOS UVA-URSI LEAF; SOLIDAGO VIRGAUREA FLOWERING TOP; BETULA PUBESCENS LEAF; EQUISETUM ARVENSE TOP; PORK KIDNEY; CYTISUS SCOPARIUS FLOWERING TOP; COPPER; PETROSELINUM CRISPUM ROOT
Active strength 4; 2; 2; 2; 2; 2; 4; 3; 6; 3; 8; 2 [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; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
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 Renes Betula
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ELYMUS REPENS ROOT 4 [hp_X]/mL ONONIS REPENS ROOT 2 [hp_X]/mL PARSLEY 2 [hp_X]/mL CAPSELLA BURSA-PASTORIS 2 [hp_X]/mL ARCTOSTAPHYLOS UVA-URSI LEAF 2 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP 2 [hp_X]/mL BETULA PUBESCENS LEAF 4 [hp_X]/mL EQUISETUM ARVENSE TOP 3 [hp_X]/mL PORK KIDNEY 6 [hp_X]/mL CYTISUS SCOPARIUS FLOWERING TOP 3 [hp_X]/mL COPPER 8 [hp_X]/mL PETROSELINUM CRISPUM ROOT 2 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 48951-8125-3 Renes Betula 60 mL in 1 BOTTLE, DROPPER LIQUID 60 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8125 RENES BETULA LIQUID [URIEL PHARMACY INC.] 5 Current NDC, Legacy NDC, 1 package rows 20210707_e7c64fc1-3e3b-478f-8b7b-c1a2b7780ba5.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 48951-8125-3 48951812503 60 mL in 1 BOTTLE, DROPPER (48951-8125-3) 60 ml 2009-09-01 0000-00-00 No No Current