Product NDC: | 10191-1251 |
Proprietary Name: | ARNICA MONTANA (WHOLE PLANT) |
Non Proprietary Name: | ARNICA WHOLE PLANT |
Active Ingredient(s): | 12 [hp_C]/1 & nbsp; ARNICA WHOLE PLANT |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10191-1251 |
Labeler Name: | Remedy Makers |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20030108 |
Package NDC: | 10191-1251-2 |
Package Description: | 162 PELLET in 1 VIAL, GLASS (10191-1251-2) |
NDC Code | 10191-1251-2 |
Proprietary Name | ARNICA MONTANA (WHOLE PLANT) |
Package Description | 162 PELLET in 1 VIAL, GLASS (10191-1251-2) |
Product NDC | 10191-1251 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARNICA WHOLE PLANT |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20030108 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Remedy Makers |
Substance Name | ARNICA MONTANA |
Strength Number | 12 |
Strength Unit | [hp_C]/1 |
Pharmaceutical Classes |