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GUNA-TF PAPILLOMA
GUNA-TF PAPILLOMA - 17089-281-10 - (HUMAN PAPILLOMAVIRUS)
Drug Information of GUNA-TF PAPILLOMA
| Product NDC: | 17089-281 |
| Proprietary Name: | GUNA-TF PAPILLOMA |
| Non Proprietary Name: | HUMAN PAPILLOMAVIRUS |
| Active Ingredient(s): | 7 [hp_X]/4600mg & nbsp; HUMAN PAPILLOMAVIRUS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUNA-TF PAPILLOMA
| Product NDC: | 17089-281 |
| Labeler Name: | Guna spa |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20080416 |
Package Information of GUNA-TF PAPILLOMA
| Package NDC: | 17089-281-10 |
| Package Description: | 1 BOTTLE in 1 BOX (17089-281-10) > 4600 mg in 1 BOTTLE |
NDC Information of GUNA-TF PAPILLOMA
| NDC Code | 17089-281-10 |
| Proprietary Name | GUNA-TF PAPILLOMA |
| Package Description | 1 BOTTLE in 1 BOX (17089-281-10) > 4600 mg in 1 BOTTLE |
| Product NDC | 17089-281 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HUMAN PAPILLOMAVIRUS |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080416 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Guna spa |
| Substance Name | HUMAN PAPILLOMAVIRUS |
| Strength Number | 7 |
| Strength Unit | [hp_X]/4600mg |
| Pharmaceutical Classes |
