Home NDC 48951-5007 Gentiana Absinthium
Product NDC 48951-5007
11-digit product format 489515007
Labeler code 48951
Product ID 48951-5007_2b250370-261d-fe8f-e063-6394a90a6423
Type HUMAN OTC DRUG
Nonproprietary name Gentiana Absinthium
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance WORMWOOD; GENTIANA LUTEA ROOT; TARAXACUM PALUSTRE ROOT; STRYCHNOS NUX-VOMICA SEED
Active strength 3; 3; 3; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
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 Gentiana Absinthium
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WORMWOOD 3 [hp_X]/mL GENTIANA LUTEA ROOT 3 [hp_X]/mL TARAXACUM PALUSTRE ROOT 3 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 6 [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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-5007-1 Gentiana Absinthium 1 mL in 1 AMPULE LIQUID 1 3 48951-5007-1 Gentiana Absinthium 10 in 1 BOX LIQUID 10 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-5007 GENTIANA ABSINTHIUM LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20250109_1b53081c-717e-46ae-8f86-e6f070c3c97d.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 48951-5007-1 48951500701 10 AMPULE in 1 BOX (48951-5007-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current