Home NDC 48951-3287 Cocculus Conium
Product NDC 48951-3287
11-digit product format 489513287
Labeler code 48951
Product ID 48951-3287_5b9c42a5-5b8e-0b29-e063-6294a90aea8a
Type HUMAN OTC DRUG
Nonproprietary name Cocculus Conium
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ANAMIRTA COCCULUS WHOLE; CONIUM MACULATUM ROOT; AMBERGRIS; LIQUID PETROLEUM
Active strength 4; 4; 7; 9 [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 Cocculus Conium
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANAMIRTA COCCULUS WHOLE 4 [hp_X]/mL CONIUM MACULATUM ROOT 4 [hp_X]/mL AMBERGRIS 7 [hp_X]/mL LIQUID PETROLEUM 9 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# 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 48951-3287-1 48951328701 10 AMPULE in 1 BOX (48951-3287-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current