Home
>
National Drug Code (NDC)
>
ARNICA MONTANA
ARNICA MONTANA - 10191-1248-2 - (ARNICA WHOLE PLANT)
Drug Information of ARNICA MONTANA
| Product NDC: | 10191-1248 |
| Proprietary Name: | ARNICA MONTANA |
| Non Proprietary Name: | ARNICA WHOLE PLANT |
| Active Ingredient(s): | 3 [hp_C]/1 & nbsp; ARNICA WHOLE PLANT |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARNICA MONTANA
| Product NDC: | 10191-1248 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20080424 |
Package Information of ARNICA MONTANA
| Package NDC: | 10191-1248-2 |
| Package Description: | 148 PELLET in 1 VIAL, GLASS (10191-1248-2) |
NDC Information of ARNICA MONTANA
| NDC Code | 10191-1248-2 |
| Proprietary Name | ARNICA MONTANA |
| Package Description | 148 PELLET in 1 VIAL, GLASS (10191-1248-2) |
| Product NDC | 10191-1248 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA WHOLE PLANT |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20080424 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | ARNICA MONTANA |
| Strength Number | 3 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
