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 |