Arnica Montana

Product NDC
80004-200
11-digit product format
800040200
Labeler code
80004
Product ID
80004-200_4e580d6f-4b9c-6c20-e063-6294a90a1d67
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana
Dosage form
TABLET
Route
ORAL
Labeler
VITAMEDICA, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-03-14
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
Brand name suffix
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
80004-200-10Arnica Montana200C HPUS1 in 1 CARTONTABLET12
80004-200-10Arnica Montana200C HPUS150 in 1 BOTTLETABLET1502
80004-200-20Arnica Montana200C HPUS30 in 1 BLISTER PACKTABLET302
80004-200-20Arnica Montana200C HPUS1 in 1 CARTONTABLET12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80004-200-10800040200101 BOTTLE in 1 CARTON (80004-200-10) / 150 TABLET in 1 BOTTLE1 bottle2022-03-14NoNoCurrent
80004-200-20800040200201 BLISTER PACK in 1 CARTON (80004-200-20) / 30 TABLET in 1 BLISTER PACK1 blister pack2022-03-14NoNoCurrent