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Herpes Zoster Remedy - 43742-0174-1 - (Herpes Zoster)

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Drug Information of Herpes Zoster Remedy

Product NDC: 43742-0174
Proprietary Name: Herpes Zoster Remedy
Non Proprietary Name: Herpes Zoster
Active Ingredient(s): 15    [hp_X]/mL & nbsp;   Herpes Zoster
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Herpes Zoster Remedy

Product NDC: 43742-0174
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121106

Package Information of Herpes Zoster Remedy

Package NDC: 43742-0174-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0174-1)

NDC Information of Herpes Zoster Remedy

NDC Code 43742-0174-1
Proprietary Name Herpes Zoster Remedy
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0174-1)
Product NDC 43742-0174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Herpes Zoster
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121106
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name HUMAN HERPESVIRUS 3
Strength Number 15
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Herpes Zoster Remedy


General Information