ARNICA MONTANA (Whole Plant)

Product NDC
10191-1255
11-digit product format
101911255
Labeler code
10191
Product ID
10191-1255_5ffbdaa5-43e0-4740-88a7-43a589dcaa8b
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA WHOLE PLANT
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
Remedy Makers
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2002-08-21
Marketing end
0000-00-00
Substance
ARNICA MONTANA
Active strength
20 [hp_M]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-1255-2ARNICA MONTANA (Whole Plant)171 in 1 VIAL, GLASSPELLET1718

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWARNICA MONTANA (WHOLE PLANT) (ARNICA WHOLE PLANT) PELLET [REMEDY MAKERS]7
ARNICA MONTANAACTIVE MOIETYO80TY208ZWARNICA MONTANA (WHOLE PLANT) (ARNICA WHOLE PLANT) PELLET [REMEDY MAKERS]7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-1255ARNICA MONTANA (WHOLE PLANT) (ARNICA WHOLE PLANT) PELLET [REMEDY MAKERS]8Legacy NDC, 1 package rows20230325_f695dfe4-3103-450a-aeef-8ea420e78df2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10191-1255-210191125502171 in 1 VIAL, GLASSHistorical