Home NDC 48951-7225 Levisticum decoction 3X
Product NDC 48951-7225
11-digit product format 489517225
Labeler code 48951
Product ID 48951-7225_535b6519-bb1a-1b32-e063-6394a90ad4ac
Type HUMAN OTC DRUG
Nonproprietary name Levisticum decoction 3X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance LEVISTICUM OFFICINALE ROOT
Active strength 3 [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 Levisticum decoction 3X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEVISTICUM OFFICINALE ROOT 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 46QZ19OEX8 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 48951-7225-3 48951722503 60 mL in 1 BOTTLE, DROPPER (48951-7225-3) 60 ml 2009-09-01 No No Current