Product NDC: | 34666-006 |
Proprietary Name: | Revitalix |
Non Proprietary Name: | China officinalis, Ferrum Phosphoricum and Medicago Sativa |
Active Ingredient(s): | 8; 8 [HP_X]/240mL; [HP_X]/240mL & nbsp; China officinalis, Ferrum Phosphoricum and Medicago Sativa |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 34666-006 |
Labeler Name: | Nartex Laboratorios Homeopaticos, S.A. De C.V. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090801 |
Package NDC: | 34666-006-80 |
Package Description: | 240 mL in 1 BOTTLE (34666-006-80) |
NDC Code | 34666-006-80 |
Proprietary Name | Revitalix |
Package Description | 240 mL in 1 BOTTLE (34666-006-80) |
Product NDC | 34666-006 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | China officinalis, Ferrum Phosphoricum and Medicago Sativa |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20090801 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Nartex Laboratorios Homeopaticos, S.A. De C.V. |
Substance Name | CINCHONA OFFICINALIS; MEDICAGO SATIVA LEAF |
Strength Number | 8; 8 |
Strength Unit | [HP_X]/240mL; [HP_X]/240mL |
Pharmaceutical Classes |