Product NDC: | 61727-302 |
Proprietary Name: | Arthritis Relief |
Non Proprietary Name: | ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF |
Active Ingredient(s): | 18; 8; 8; 8; 8; 8 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp; ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61727-302 |
Labeler Name: | Homeocare Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120731 |
Package NDC: | 61727-302-21 |
Package Description: | 4 g in 1 TUBE (61727-302-21) |
NDC Code | 61727-302-21 |
Proprietary Name | Arthritis Relief |
Package Description | 4 g in 1 TUBE (61727-302-21) |
Product NDC | 61727-302 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARNICA MONTANA, BRYONIA ALBA, CHAMOMILLA,HYPERICUM PERFORATUM, KALMIA LATIFOLIA LEAF,KALMIA LATIFOLIA LEAF |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20120731 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Homeocare Laboratories |
Substance Name | ARNICA MONTANA; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM; KALMIA LATIFOLIA LEAF; MATRICARIA RECUTITA; TOXICODENDRON PUBESCENS LEAF |
Strength Number | 18; 8; 8; 8; 8; 8 |
Strength Unit | [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g |
Pharmaceutical Classes |