Home NDC 48951-3032 Carduus Viscum
Product NDC 48951-3032
11-digit product format 489513032
Labeler code 48951
Product ID 48951-3032_5a9929f6-2133-b766-e063-6394a90aa442
Type HUMAN OTC DRUG
Nonproprietary name Carduus Viscum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance MILK THISTLE; VISCUM ALBUM FRUITING TOP; MAMMAL LIVER
Active strength 3; 4; 8 [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 Carduus Viscum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MILK THISTLE 3 [hp_X]/mL VISCUM ALBUM FRUITING TOP 4 [hp_X]/mL MAMMAL LIVER 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U946SH95EE Internal UNII lookup BK9092J5MP Internal UNII lookup
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 48951-3032-1 Carduus Viscum 1 mL in 1 AMPULE LIQUID 1 4 48951-3032-1 Carduus Viscum 10 in 1 BOX LIQUID 10 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3032 CARDUUS VISCUM LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20241208_ec3bdc80-ecb4-4ec6-bb64-37a5cd344a39.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 48951-3032-1 48951303201 10 AMPULE in 1 BOX (48951-3032-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current