Arnica montana

Product NDC
0220-0449
11-digit product format
002200449
Labeler code
0220
Product ID
0220-0449_471d8d0e-8753-5063-e063-6394a90a2dcc
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
12 [hp_X]/12[hp_X]
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 MONTANA12 [hp_X]/12[hp_X]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0449-412023-06-26C16284748780-1f386c649-b5b8-0266-e053-dadaa90a7c1aArnica montana 12X
0220-0449-412023-01-30C16284748780-1f386c649-b5b8-0266-e053-dadaa90a7c1aArnica montana 12X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0449-41Arnica montana12 [hp_X] in 1 TUBEPELLET123

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0449ARNICA MONTANA (ARNICA MONTANA ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230627_84eebf11-d58c-1e9f-e053-2991aa0a9cf3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0449-410022004494112 [hp_X] in 1 TUBE (0220-0449-41) 1983-03-030000-00-00NoNoCurrent