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