Home NDC 48951-1106 Arnica Aurum 20/30
Product NDC 48951-1106
11-digit product format 489511106
Labeler code 48951
Product ID 48951-1106_44840be2-b7bb-ba38-e063-6394a90a0e38
Type HUMAN OTC DRUG
Nonproprietary name Arnica Aurum 20/30
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ARNICA MONTANA; GOLD; HYOSCYAMUS NIGER LEAF; ONOPORDUM ACANTHIUM FLOWER; PRIMULA VERIS FLOWER
Active strength 20; 30; 4; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnica Aurum 20/30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ONOPORDUM ACANTHIUM FLOWER 20 [hp_X]/mL PRIMULA VERIS FLOWER 30 [hp_X]/mL HYOSCYAMUS NIGER LEAF 4 [hp_X]/mL ARNICA MONTANA 3 [hp_X]/mL GOLD 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 48951-1106-1 Arnica Aurum 20/30 1 mL in 1 AMPULE LIQUID 1 5 48951-1106-1 Arnica Aurum 20/30 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 48951-1106 ARNICA AURUM 20/30 LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20240120_9ebdcfa6-f8b1-4a25-9008-e9f923ec9ffd.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 48951-1106-1 48951110601 10 AMPULE in 1 BOX (48951-1106-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current