Arnica montana

Product NDC
0220-0514
11-digit product format
002200514
Labeler code
0220
Product ID
0220-0514_471d1b58-e0b2-e07d-e063-6394a90ab3ec
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
ARNICA MONTANA
Active strength
10 [hp_M]/10[hp_M]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnica montana
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA10 [hp_M]/10[hp_M]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0514-412023-04-11C16284748780-1f386c64a-2dfd-0266-e053-dadaa90a7c1aArnica montana 10M
0220-0514-412023-01-30C16284748780-1f386c64a-2dfd-0266-e053-dadaa90a7c1aArnica montana 10M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0514-41Arnica montana10 [hp_M] in 1 TUBEPELLET103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0514ARNICA MONTANA (ARNICA MONTANA ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230412_84eeabc1-1c42-08fd-e053-2a91aa0aab44.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0514-410022005144110 [hp_M] in 1 TUBE (0220-0514-41) 1983-03-030000-00-00NoNoCurrent