Energize - 57520-0058-1 - (Energize)

Alphabetical Index


Drug Information of Energize

Product NDC: 57520-0058
Proprietary Name: Energize
Non Proprietary Name: Energize
Active Ingredient(s): 6; 3; 3; 6; 12; 6    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Energize
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Energize

Product NDC: 57520-0058
Labeler Name: Apothica Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100125

Package Information of Energize

Package NDC: 57520-0058-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0058-1)

NDC Information of Energize

NDC Code 57520-0058-1
Proprietary Name Energize
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0058-1)
Product NDC 57520-0058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Energize
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100125
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apothica Company
Substance Name AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GINGER; PHOSPHORIC ACID; POTASSIUM PHOSPHATE, DIBASIC; TRINITROPHENOL
Strength Number 6; 3; 3; 6; 12; 6
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Food Additives [Chemical/Ingredient],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Energize


General Information