Product NDC: | 17089-269 |
Proprietary Name: | GUNA-TF HERPES |
Non Proprietary Name: | HUMAN HERPESVIRUS 1 - HUMAN HERPESVIRUS 2 - |
Active Ingredient(s): | 7; 7 [hp_X]/4600mg; [hp_X]/4600mg & nbsp; HUMAN HERPESVIRUS 1 - HUMAN HERPESVIRUS 2 - |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17089-269 |
Labeler Name: | Guna spa |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20060523 |
Package NDC: | 17089-269-10 |
Package Description: | 1 BOTTLE in 1 BOX (17089-269-10) > 4600 mg in 1 BOTTLE |
NDC Code | 17089-269-10 |
Proprietary Name | GUNA-TF HERPES |
Package Description | 1 BOTTLE in 1 BOX (17089-269-10) > 4600 mg in 1 BOTTLE |
Product NDC | 17089-269 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HUMAN HERPESVIRUS 1 - HUMAN HERPESVIRUS 2 - |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20060523 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Guna spa |
Substance Name | HUMAN HERPESVIRUS 1; HUMAN HERPESVIRUS 2 |
Strength Number | 7; 7 |
Strength Unit | [hp_X]/4600mg; [hp_X]/4600mg |
Pharmaceutical Classes |