Product NDC: | 53499-3533 |
Proprietary Name: | Arnica Montana |
Non Proprietary Name: | Arnica Montana |
Active Ingredient(s): | 6 [hp_X]/1 & nbsp; Arnica Montana |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53499-3533 |
Labeler Name: | Nature's Way Holding Co |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20060101 |
Package NDC: | 53499-3533-3 |
Package Description: | 250 TABLET in 1 BOTTLE, GLASS (53499-3533-3) |
NDC Code | 53499-3533-3 |
Proprietary Name | Arnica Montana |
Package Description | 250 TABLET in 1 BOTTLE, GLASS (53499-3533-3) |
Product NDC | 53499-3533 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Arnica Montana |
Dosage Form Name | TABLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20060101 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Nature's Way Holding Co |
Substance Name | ARNICA MONTANA |
Strength Number | 6 |
Strength Unit | [hp_X]/1 |
Pharmaceutical Classes |