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Cerebroforce - 57520-0065-1 - (Cerebroforce)

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Drug Information of Cerebroforce

Product NDC: 57520-0065
Proprietary Name: Cerebroforce
Non Proprietary Name: Cerebroforce
Active Ingredient(s): 30; 3; 12; 3; 12; 12; 12    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Cerebroforce
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Cerebroforce

Product NDC: 57520-0065
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100208

Package Information of Cerebroforce

Package NDC: 57520-0065-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0065-1)

NDC Information of Cerebroforce

NDC Code 57520-0065-1
Proprietary Name Cerebroforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0065-1)
Product NDC 57520-0065
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cerebroforce
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100208
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ARSENIC TRIOXIDE; CHILI PEPPER; GELSEMIUM SEMPERVIRENS ROOT; GINKGO; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; POTASSIUM PHOSPHATE, DIBASIC
Strength Number 30; 3; 12; 3; 12; 12; 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 Cerebroforce


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