Product NDC: | 43689-0003 |
Proprietary Name: | Fibromyalgia Relief |
Non Proprietary Name: | Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum |
Active Ingredient(s): | 30; 30; 30; 30; 30; 3; 30; 30; 30; 30; 30 [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_X]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg & nbsp; Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43689-0003 |
Labeler Name: | The Magni Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20121011 |
Package NDC: | 43689-0003-1 |
Package Description: | 125 mg in 1 BOTTLE (43689-0003-1) |
NDC Code | 43689-0003-1 |
Proprietary Name | Fibromyalgia Relief |
Package Description | 125 mg in 1 BOTTLE (43689-0003-1) |
Product NDC | 43689-0003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121011 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | The Magni Company |
Substance Name | ACONITUM NAPELLUS; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CONIINE; GELSEMIUM SEMPERVIRENS ROOT; HYPERICUM PERFORATUM; LACTIC ACID, DL-; PHOSPHORIC ACID; POTASSIUM DICHROMATE; TOXICODENDRON PUBESCENS LEAF; URIC ACID |
Strength Number | 30; 30; 30; 30; 30; 3; 30; 30; 30; 30; 30 |
Strength Unit | [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_X]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg |
Pharmaceutical Classes |