Home NDC 48951-1411 Arnica Aurum 20/30
Product NDC 48951-1411
11-digit product format 489511411
Labeler code 48951
Product ID 48951-1411_5725bfe1-1e13-561e-e063-6294a90aedfc
Type HUMAN OTC DRUG
Nonproprietary name Arnica Aurum 20/30
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ARNICA MONTANA; GOLD
Active strength 20; 30 [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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 Arnica Aurum 20/30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 20 [hp_X]/1 GOLD 30 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O80TY208ZW Internal UNII lookup 79Y1949PYO Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Socrata Ingredients# 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 48951-1411-2 48951141102 1350 PELLET in 1 BOTTLE, GLASS (48951-1411-2) 1350 pellet 2009-09-01 No No Current