Revitalix - 34666-006-80 - (China officinalis, Ferrum Phosphoricum and Medicago Sativa)

Alphabetical Index


Drug Information of Revitalix

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)

Labeler Information of Revitalix

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 Information of Revitalix

Package NDC: 34666-006-80
Package Description: 240 mL in 1 BOTTLE (34666-006-80)

NDC Information of Revitalix

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

Complete Information of Revitalix


General Information