NDC 17089-281

GUNA-TF PAPILLOMA

Human Papillomavirus

GUNA-TF PAPILLOMA is a Oral Capsule, Gelatin Coated in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Human Papillomavirus.

• Product ID: 17089-281_69423426-fa1c-4b19-bbe5-fe63ddb688e4
• NDC: 17089-281
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-TF PAPILLOMA
• Generic Name: Human Papillomavirus
• Dosage Form: Capsule, Gelatin Coated
• Route of Administration: ORAL
• Marketing Start Date: 2008-04-16
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: HUMAN PAPILLOMAVIRUS
• Active Ingredient Strength: 7 [hp_X]/4600mg
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 17089-281-10

1 BOTTLE in 1 BOX (17089-281-10) > 4600 mg in 1 BOTTLE

• Marketing Start Date: 2008-04-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-281-10 [17089028110]

GUNA-TF PAPILLOMA CAPSULE, GELATIN COATED

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2008-04-16
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
HUMAN PAPILLOMAVIRUS	7 [hp_X]/4600mg

OpenFDA Data

• SPL SET ID: 9badc0cf-f62c-4444-a66d-1204c3397bb7
• Manufacturer:
  • Guna spa
• UNII:
  • 23CVL7WF4J