ARNICA

Product NDC: 54973-3084
11-digit product format: 549733084
Labeler code: 54973
Product ID: 54973-3084_326e4d6c-5a9b-42f2-e063-6294a90ab51c
Type: HUMAN OTC DRUG
Nonproprietary name: arnica montana
Dosage form: TABLET, SOLUBLE
Route: ORAL
Labeler: Hyland's Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2008-12-17
Substance: ARNICA MONTANA
Active strength: 30 [hp_X]/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	54973-3084	54973-3084-1	D	Discontinued by firm		2026-08-03
excluded package	package	54973-3084	54973-3084-3	D	Discontinued by firm		2026-08-03

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 14 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	54973-3084-3	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	54973-3084-1	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	54973-3084-3	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	54973-3084-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	54973-3084-1	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	54973-3084-3	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	54973-3084-1	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	54973-3084-3	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	54973-3084-1	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	54973-3084-3	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	54973-3084-1	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	54973-3084-3	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	54973-3084-1	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	54973-3084-3	`302b2466d912…`	`e7b80fea0513…`

Additional Listing Data#

Finished product: Yes
Brand name base: ARNICA
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ARNICA MONTANA	30 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
O80TY208ZW	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
85fcf1c8-6f89-4862-85a8-4983cbea28f4	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
54973-3084-1	ARNICA	50 in 1 BOTTLE, PLASTIC	TABLET, SOLUBLE	50	12
54973-3084-3	ARNICA	4 in 1 PACKET	TABLET, SOLUBLE	4	12
54973-3084-5	ARNICA	100 in 1 BOTTLE, PLASTIC	TABLET, SOLUBLE	100	12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ARNICA MONTANA	ACTIVE INGREDIENT	O80TY208ZW	ARNICA (ARNICA MONTANA) TABLET, SOLUBLE [HYLAND'S]	2
ARNICA MONTANA	ACTIVE MOIETY	O80TY208ZW	ARNICA (ARNICA MONTANA) TABLET, SOLUBLE [HYLAND'S]	2
ACACIA	INACTIVE INGREDIENT	5C5403N26O	ARNICA (ARNICA MONTANA) TABLET, SOLUBLE [HYLAND'S]	2
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ARNICA (ARNICA MONTANA) TABLET, SOLUBLE [HYLAND'S]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54973-3084	ARNICA (ARNICA MONTANA) TABLET, SOLUBLE [HYLAND'S INC.]	12	Current NDC, Legacy NDC, 3 package rows	20250411_85fcf1c8-6f89-4862-85a8-4983cbea28f4.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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ARNICA	ARNICA MONTANA	Hyland's Inc.	85fcf1c8-6f89-4862-85a8-4983cbea28f4	2026-07-16	Warnings	Exact identifier ndc (product): 54973-3084

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O80TY208ZW	ARNICA MONTANA	8057-65-6	ARNICA MONTANA

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
54973-3084-1	54973308401	50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-3084-1)	2008-12-17	0000-00-00	No	No	Current
54973-3084-3	54973308403	4 TABLET, SOLUBLE in 1 PACKET (54973-3084-3)	2008-12-17	0000-00-00	No	No	Current
54973-3084-5	54973308405	100 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-3084-5)	2008-12-17	0000-00-00	No	No	Current