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