Arnica

Product NDC
44911-0241
11-digit product format
449110241
Labeler code
44911
Product ID
44911-0241_2924f180-600e-479f-9b97-831d824a00c7
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-08-11
Substance
ARNICA MONTANA
Active strength
200 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA200 [hp_C]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0241-1Arnica30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0241ARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20181025_96259b60-cd7f-40d9-a3d4-6a41a6e04f1e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0241-14491102410130 mL in 1 BOTTLE, DROPPER (44911-0241-1) 30 ml2015-08-110000-00-00NoNoCurrent