Product NDC: | 50114-2316 |
Proprietary Name: | Arnica PC |
Non Proprietary Name: | ARNICA MONTANA ROOT |
Active Ingredient(s): | 6 [hp_X]/300mg & nbsp; ARNICA MONTANA ROOT |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-2316 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20000131 |
Package NDC: | 50114-2316-2 |
Package Description: | 30000 mg in 1 BOTTLE (50114-2316-2) |
NDC Code | 50114-2316-2 |
Proprietary Name | Arnica PC |
Package Description | 30000 mg in 1 BOTTLE (50114-2316-2) |
Product NDC | 50114-2316 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARNICA MONTANA ROOT |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20000131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | ARNICA MONTANA ROOT |
Strength Number | 6 |
Strength Unit | [hp_X]/300mg |
Pharmaceutical Classes |