| Product NDC: | 61657-0965 |
| Proprietary Name: | Total Uranium |
| Non Proprietary Name: | Uranium Nitricum |
| Active Ingredient(s): | 15 [hp_X]/30mL & nbsp; Uranium Nitricum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61657-0965 |
| Labeler Name: | White Manufacturing Inc, DBA Micro-West |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110801 |
| Package NDC: | 61657-0965-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (61657-0965-1) |
| NDC Code | 61657-0965-1 |
| Proprietary Name | Total Uranium |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (61657-0965-1) |
| Product NDC | 61657-0965 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Uranium Nitricum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | White Manufacturing Inc, DBA Micro-West |
| Substance Name | URANYL NITRATE HEXAHYDRATE |
| Strength Number | 15 |
| Strength Unit | [hp_X]/30mL |
| Pharmaceutical Classes |