NDC 17089-456

GUNA-INF ALPHA

Interferon Alfa-2a

GUNA-INF ALPHA is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Interferon Alfa-2a.

• Product ID: 17089-456_7e91f7fb-2a2f-4682-e053-2991aa0a1c5c
• NDC: 17089-456
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-INF ALPHA
• Generic Name: Interferon Alfa-2a
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2011-02-16
• Marketing End Date: 2021-07-31
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: INTERFERON ALFA-2A
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N

Packaging

NDC 17089-456-18

1 BOTTLE, DROPPER in 1 BOX (17089-456-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2011-02-16
• Marketing End Date: 2021-07-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-456-18 [17089045618]

GUNA-INF ALPHA SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-02-16
• Marketing End Date: 2021-07-31

Drug Details

Active Ingredients

Ingredient	Strength
INTERFERON ALFA-2A	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: f96495b5-1ffe-432c-adcf-b2db9cfd1405
• Manufacturer:
  • Guna spa
• UNII:
  • 47RRR83SK7
• UPC Code:
  • 0317089456186