NDC 17089-372

GUNA-EGF

Epidermal Growth Factor

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

• Product ID: 17089-372_82de46fa-983c-fade-e053-2991aa0aea95
• NDC: 17089-372
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-EGF
• Generic Name: Epidermal 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: HUMAN EPIDERMAL GROWTH FACTOR
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 17089-372-18

1 BOTTLE, DROPPER in 1 BOX (17089-372-18) > 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 17089-372-18 [17089037218]

GUNA-EGF SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-03-31

Drug Details

Active Ingredients

Ingredient	Strength
HUMAN EPIDERMAL GROWTH FACTOR	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: 6473bd71-5baf-4c42-ac0b-2cfaf69bfd8c
• Manufacturer:
  • Guna spa
• UNII:
  • TZK30RF92W
• UPC Code:
  • 0317089372189