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Super Viragon - 75830-001-59 - (Bryonia Alba, Pulsatilla)

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Drug Information of Super Viragon

Product NDC: 75830-001
Proprietary Name: Super Viragon
Non Proprietary Name: Bryonia Alba, Pulsatilla
Active Ingredient(s): 30; 30    [hp_X]/59mL; [hp_X]/59mL & nbsp;   Bryonia Alba, Pulsatilla
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Super Viragon

Product NDC: 75830-001
Labeler Name: Baseline Nutritionals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110701

Package Information of Super Viragon

Package NDC: 75830-001-59
Package Description: 59 mL in 1 BOTTLE, DROPPER (75830-001-59)

NDC Information of Super Viragon

NDC Code 75830-001-59
Proprietary Name Super Viragon
Package Description 59 mL in 1 BOTTLE, DROPPER (75830-001-59)
Product NDC 75830-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bryonia Alba, Pulsatilla
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110701
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Baseline Nutritionals Inc.
Substance Name BRYONIA ALBA ROOT; PULSATILLA VULGARIS
Strength Number 30; 30
Strength Unit [hp_X]/59mL; [hp_X]/59mL
Pharmaceutical Classes

Complete Information of Super Viragon


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