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Arterioforce - 57520-0510-1 - (Baptisia tinctoria, Echinacea, Hydrastis canadensis)

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Drug Information of Arterioforce

Product NDC: 57520-0510
Proprietary Name: Arterioforce
Non Proprietary Name: Baptisia tinctoria, Echinacea, Hydrastis canadensis
Active Ingredient(s): 6; 3; 12; 12; 12; 3; 4; 3; 4; 3; 5; 6; 4; 6    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Baptisia tinctoria, Echinacea, Hydrastis canadensis
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Arterioforce

Product NDC: 57520-0510
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100624

Package Information of Arterioforce

Package NDC: 57520-0510-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0510-1)

NDC Information of Arterioforce

NDC Code 57520-0510-1
Proprietary Name Arterioforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0510-1)
Product NDC 57520-0510
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Baptisia tinctoria, Echinacea, Hydrastis canadensis
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100624
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ARNICA MONTANA; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; CONIUM MACULATUM FLOWERING TOP; ECHINACEA; FENUGREEK SEED; GOLDENSEAL; MYRRH; PHYTOLACCA AMERICANA ROOT; POTASSIUM IODIDE; PROPOLIS WAX; RORIPPA NASTURTIUM-AQUATICUM; SELENICEREUS GRANDIFLORUS STEM
Strength Number 6; 3; 12; 12; 12; 3; 4; 3; 4; 3; 5; 6; 4; 6
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 Arterioforce


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