NDC 17089-382

GUNA-IL 4

Binetrakin

GUNA-IL 4 is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Binetrakin.

• Product ID: 17089-382_7dd65a43-605c-1f16-e053-2a91aa0a466d
• NDC: 17089-382
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-IL 4
• Generic Name: Binetrakin
• 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: BINETRAKIN
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-382-18

1 BOTTLE, DROPPER in 1 BOX (17089-382-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2008-06-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-382-18 [17089038218]

GUNA-IL 4 SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2008-06-17
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
BINETRAKIN	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: da1f5fe8-508d-4911-804a-8489ca97e071
• Manufacturer:
  • Guna spa
• UNII:
  • 751635Z921
• UPC Code:
  • 0317089382188