Product NDC: | 10191-1242 |
Proprietary Name: | ARNICA MONTANA |
Non Proprietary Name: | WHOLE ARNICA PLANT |
Active Ingredient(s): | 6 [hp_X]/1 & nbsp; WHOLE ARNICA PLANT |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10191-1242 |
Labeler Name: | Remedy Makers |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20030806 |
Package NDC: | 10191-1242-2 |
Package Description: | 164 PELLET in 1 VIAL, GLASS (10191-1242-2) |
NDC Code | 10191-1242-2 |
Proprietary Name | ARNICA MONTANA |
Package Description | 164 PELLET in 1 VIAL, GLASS (10191-1242-2) |
Product NDC | 10191-1242 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | WHOLE ARNICA PLANT |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20030806 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Remedy Makers |
Substance Name | ARNICA MONTANA |
Strength Number | 6 |
Strength Unit | [hp_X]/1 |
Pharmaceutical Classes |