Arnica Aurum 20/30

Product NDC: 48951-1411
Requested package NDC: 48951-1411-2
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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
bf5c7dfe-ffc1-43f2-b00d-92fa7b014bea	Available on FDA.report

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ARNICA MONTANA	ACTIVE INGREDIENT	O80TY208ZW	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
GOLD	ACTIVE INGREDIENT	79Y1949PYO	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
HYOSCYAMUS NIGER LEAF	ACTIVE INGREDIENT	32IT7G8BAW	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
ONOPORDUM ACANTHIUM FLOWER	ACTIVE INGREDIENT	AP97AUF88E	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
PRIMULA VERIS FLOWER	ACTIVE INGREDIENT	W5BET37294	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
ARNICA MONTANA	ACTIVE MOIETY	O80TY208ZW	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
GOLD	ACTIVE MOIETY	79Y1949PYO	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
HYOSCYAMUS NIGER LEAF	ACTIVE MOIETY	32IT7G8BAW	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
ONOPORDUM ACANTHIUM FLOWER	ACTIVE MOIETY	AP97AUF88E	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
PRIMULA VERIS FLOWER	ACTIVE MOIETY	W5BET37294	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	ARNICA AURUM 20/30 PELLET [URIEL PHARMACY INC.]	1

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Arnica Aurum 20/30	ARNICA AURUM 20/30	Uriel Pharmacy Inc.	bf5c7dfe-ffc1-43f2-b00d-92fa7b014bea	2026-07-21	Warnings	Exact identifier ndc (package): 48951-1411-2 ndc (product): 48951-1411 ndc11 (package): 48951141102

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O80TY208ZW	ARNICA MONTANA	8057-65-6	ARNICA MONTANA
79Y1949PYO	GOLD	7440-57-5	GOLD

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