Home > National Drug Code (NDC) > Albuminuriaforce

Albuminuriaforce - 57520-0459-1 - (Equisetum hyemale, Solidago virgaurea, Apis mellifica, Mercurius corrosivus, Nux moschata, Phosphorus, Terebinthina,)

Alphabetical Index


Drug Information of Albuminuriaforce

Product NDC: 57520-0459
Proprietary Name: Albuminuriaforce
Non Proprietary Name: Equisetum hyemale, Solidago virgaurea, Apis mellifica, Mercurius corrosivus, Nux moschata, Phosphorus, Terebinthina,
Active Ingredient(s): 12; 3; 12; 12; 12; 3; 12    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Equisetum hyemale, Solidago virgaurea, Apis mellifica, Mercurius corrosivus, Nux moschata, Phosphorus, Terebinthina,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Albuminuriaforce

Product NDC: 57520-0459
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100603

Package Information of Albuminuriaforce

Package NDC: 57520-0459-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0459-1)

NDC Information of Albuminuriaforce

NDC Code 57520-0459-1
Proprietary Name Albuminuriaforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0459-1)
Product NDC 57520-0459
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Equisetum hyemale, Solidago virgaurea, Apis mellifica, Mercurius corrosivus, Nux moschata, Phosphorus, Terebinthina,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100603
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name APIS MELLIFERA; EQUISETUM HYEMALE; MERCURIC CHLORIDE; NUTMEG; PHOSPHORUS; SOLIDAGO VIRGAUREA FLOWERING TOP; TURPENTINE
Strength Number 12; 3; 12; 12; 12; 3; 12
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Albuminuriaforce


General Information