| Product NDC: | 43742-0157 |
| Proprietary Name: | Joint Pain |
| Non Proprietary Name: | Arnica Montana, Bryonia, Causticum, Rhus Toxicodendron, Ferrum Phosphoricum |
| Active Ingredient(s): | 4; 4; 4; 8; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Arnica Montana, Bryonia, Causticum, Rhus Toxicodendron, Ferrum Phosphoricum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43742-0157 |
| Labeler Name: | Deseret Biologicals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120920 |
| Package NDC: | 43742-0157-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0157-1) |
| NDC Code | 43742-0157-1 |
| Proprietary Name | Joint Pain |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0157-1) |
| Product NDC | 43742-0157 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Arnica Montana, Bryonia, Causticum, Rhus Toxicodendron, Ferrum Phosphoricum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120920 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Deseret Biologicals, Inc. |
| Substance Name | ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM; FERRUM PHOSPHORICUM; TOXICODENDRON PUBESCENS LEAF |
| Strength Number | 4; 4; 4; 8; 6 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |