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GUNA-TF HERPES - 17089-269-10 - (HUMAN HERPESVIRUS 1 - HUMAN HERPESVIRUS 2 -)

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Drug Information of GUNA-TF HERPES

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)

Labeler Information of GUNA-TF HERPES

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 Information of GUNA-TF HERPES

Package NDC: 17089-269-10
Package Description: 1 BOTTLE in 1 BOX (17089-269-10) > 4600 mg in 1 BOTTLE

NDC Information of GUNA-TF HERPES

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

Complete Information of GUNA-TF HERPES


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