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Gynobalance - 57520-0104-1 - (Gynobalance)

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Drug Information of Gynobalance

Product NDC: 57520-0104
Proprietary Name: Gynobalance
Non Proprietary Name: Gynobalance
Active Ingredient(s): 8; 6; 8; 8; 8    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Gynobalance
Administration Route(s): ORAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Gynobalance

Product NDC: 57520-0104
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100218

Package Information of Gynobalance

Package NDC: 57520-0104-1
Package Description: 30 mL in 1 BOTTLE, SPRAY (57520-0104-1)

NDC Information of Gynobalance

NDC Code 57520-0104-1
Proprietary Name Gynobalance
Package Description 30 mL in 1 BOTTLE, SPRAY (57520-0104-1)
Product NDC 57520-0104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Gynobalance
Dosage Form Name SPRAY
Route Name ORAL
Start Marketing Date 20100218
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ESTRADIOL; PRASTERONE; PREGNENOLONE; PROGESTERONE; TESTOSTERONE
Strength Number 8; 6; 8; 8; 8
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Gynobalance


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