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Endocrine Balancer - 57520-0092-1 - (Endocrine Balancer)

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Drug Information of Endocrine Balancer

Product NDC: 57520-0092
Proprietary Name: Endocrine Balancer
Non Proprietary Name: Endocrine Balancer
Active Ingredient(s): 3; 3; 12; 6; 3; 6; 8    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Endocrine Balancer
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Endocrine Balancer

Product NDC: 57520-0092
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100215

Package Information of Endocrine Balancer

Package NDC: 57520-0092-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0092-1)

NDC Information of Endocrine Balancer

NDC Code 57520-0092-1
Proprietary Name Endocrine Balancer
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0092-1)
Product NDC 57520-0092
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Endocrine Balancer
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100215
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name FUCUS VESICULOSUS; GLYCYRRHIZA GLABRA; IODINE; PINUS SYLVESTRIS TOP; SARSAPARILLA; SUS SCROFA ADRENAL GLAND; THYROID
Strength Number 3; 3; 12; 6; 3; 6; 8
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 Endocrine Balancer


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