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Herpes Simplex Remedy - 43742-0182-1 - (Herpes Simplex I, Herpes Simplex II)

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Drug Information of Herpes Simplex Remedy

Product NDC: 43742-0182
Proprietary Name: Herpes Simplex Remedy
Non Proprietary Name: Herpes Simplex I, Herpes Simplex II
Active Ingredient(s): 15; 15    [hp_X]/mL; [hp_X]/mL & nbsp;   Herpes Simplex I, Herpes Simplex II
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Herpes Simplex Remedy

Product NDC: 43742-0182
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121012

Package Information of Herpes Simplex Remedy

Package NDC: 43742-0182-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0182-1)

NDC Information of Herpes Simplex Remedy

NDC Code 43742-0182-1
Proprietary Name Herpes Simplex Remedy
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0182-1)
Product NDC 43742-0182
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Herpes Simplex I, Herpes Simplex II
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121012
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name HUMAN HERPESVIRUS 1; HUMAN HERPESVIRUS 2
Strength Number 15; 15
Strength Unit [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Herpes Simplex Remedy


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