| Product NDC: | 44911-0042 |
| Proprietary Name: | Ferrum Phos |
| Non Proprietary Name: | Ferrum Phosphoricum |
| Active Ingredient(s): | 30 [hp_C]/mL & nbsp; Ferrum Phosphoricum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44911-0042 |
| Labeler Name: | Energique, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20121002 |
| Package NDC: | 44911-0042-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (44911-0042-1) |
| NDC Code | 44911-0042-1 |
| Proprietary Name | Ferrum Phos |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (44911-0042-1) |
| Product NDC | 44911-0042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ferrum Phosphoricum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121002 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Energique, Inc. |
| Substance Name | FERRUM PHOSPHORICUM |
| Strength Number | 30 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |