Home NDC 48951-8140 Rhus Aconitum
Product NDC 48951-8140
11-digit product format 489518140
Labeler code 48951
Product ID 48951-8140_4bd37192-f7e8-b961-e063-6294a90ab3d3
Type HUMAN OTC DRUG
Nonproprietary name Rhus Aconitum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance GELSEMIUM SEMPERVIRENS ROOT; PSEUDOGNAPHALIUM LUTEOALBUM LEAF; ACONITUM NAPELLUS; ATROPA BELLADONNA; MANDRAGORA OFFICINARUM ROOT; TOXICODENDRON PUBESCENS LEAF; PENOXSULAM
Active strength 4; 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
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 Rhus Aconitum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GELSEMIUM SEMPERVIRENS ROOT 4 [hp_X]/mL PSEUDOGNAPHALIUM LUTEOALBUM LEAF 4 [hp_X]/mL ACONITUM NAPELLUS 6 [hp_X]/mL ATROPA BELLADONNA 6 [hp_X]/mL MANDRAGORA OFFICINARUM ROOT 6 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL PENOXSULAM 10 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 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 48951-8140-1 Rhus Aconitum 1 mL in 1 AMPULE LIQUID 1 5 48951-8140-1 Rhus Aconitum 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 48951-8140 RHUS ACONITUM LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20240120_a176c241-fc2d-4fea-82d9-81183971b4cf.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 48951-8140-1 48951814001 10 AMPULE in 1 BOX (48951-8140-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current