Product NDC: | 61727-321 |
Proprietary Name: | Fibromyalgia Relief |
Non Proprietary Name: | ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE. |
Active Ingredient(s): | 18; 10; 10; 10; 10; 10 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp; ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE. |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61727-321 |
Labeler Name: | Homeocare Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120709 |
Package NDC: | 61727-321-21 |
Package Description: | 4 g in 1 TUBE (61727-321-21) |
NDC Code | 61727-321-21 |
Proprietary Name | Fibromyalgia Relief |
Package Description | 4 g in 1 TUBE (61727-321-21) |
Product NDC | 61727-321 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARNICA MONTANA,LACTIC ACID,STRYCHNOS NUX-VOMICA SEED,POTASSIUM PHOSPHATE, DIBASIC,CUPRIC ARSENITE. |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20120709 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Homeocare Laboratories |
Substance Name | ARNICA MONTANA; CUPRIC ARSENITE; LACTIC ACID; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; POTASSIUM PHOSPHATE, DIBASIC; STRYCHNOS NUX-VOMICA SEED |
Strength Number | 18; 10; 10; 10; 10; 10 |
Strength Unit | [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g |
Pharmaceutical Classes |