NDC 17089-390

GUNA-IL 12

Interleukin-12 Human Recombinant

GUNA-IL 12 is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Interleukin-12 Human Recombinant.

• Product ID: 17089-390_7dd767e9-959a-ee38-e053-2a91aa0ad7fe
• NDC: 17089-390
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-IL 12
• Generic Name: Interleukin-12 Human Recombinant
• 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-12 HUMAN RECOMBINANT
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-390-18

1 BOTTLE, DROPPER in 1 BOX (17089-390-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2010-06-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-390-18 [17089039018]

GUNA-IL 12 SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-06-10
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
INTERLEUKIN-12 HUMAN RECOMBINANT	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: 6a2513f0-cda9-4121-9581-5fd9078bd299
• Manufacturer:
  • Guna spa
• UNII:
  • 02FXP10O2U
• UPC Code:
  • 0317089390183