NDC 17089-381

GUNA-IL 3

Interleukin-3

GUNA-IL 3 is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Interleukin-3.

• Product ID: 17089-381_7dd767e9-95b8-ee38-e053-2a91aa0ad7fe
• NDC: 17089-381
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-IL 3
• Generic Name: Interleukin-3
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2008-06-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: INTERLEUKIN-3
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-381-18

1 BOTTLE, DROPPER in 1 BOX (17089-381-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2010-05-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-381-18 [17089038118]

GUNA-IL 3 SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-27
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
INTERLEUKIN-3	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: 5be3096f-9046-457c-b7ba-767ffe74c07a
• Manufacturer:
  • Guna spa
• UNII:
  • A802907MI4
• UPC Code:
  • 0317089381181