NDC 17089-373

GUNA-FGF

Fibroblast Growth Factor

GUNA-FGF is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Velafermin.

• Product ID: 17089-373_7dd65a43-6070-1f16-e053-2a91aa0a466d
• NDC: 17089-373
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-FGF
• Generic Name: Fibroblast Growth Factor
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2011-03-31
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: VELAFERMIN
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-373-18

1 BOTTLE, DROPPER in 1 BOX (17089-373-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2011-03-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-373-18 [17089037318]

GUNA-FGF SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-03-31
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
VELAFERMIN	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: c6beb454-5661-4d85-a6ba-b1971eda8965
• Manufacturer:
  • Guna spa
• UNII:
  • 6Z25C35927
• UPC Code:
  • 0317089373186