Arnica Montana 200C HPUS

Product NDC
80004-009
11-digit product format
800040009
Labeler code
80004
Product ID
80004-009_b9334ab5-3aa7-4e02-a6f9-414d1614ad2e
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana
Dosage form
TABLET
Route
ORAL
Labeler
VITAMEDICA, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-01-23
Substance
ARNICA MONTANA WHOLE
Active strength
200 [hp_C]/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnica Montana 200C HPUS
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80004-009-20Arnica Montana 200C HPUS150 in 1 BOTTLETABLET1501

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80004-009-2080004000920150 TABLET in 1 BOTTLE (80004-009-20) 150 tablet2026-01-23NoNoCurrent