NDC 17089-076

CITOMIX

Aldesleukin - Binetrakin - Canakinumab - Centella Asiatica - Cranberry - Human Interleukin-6 (nonglycosylated) - Interferon Gamma-1b - Lenograstim - Pineapple - Sus Scrofa Bone Marrow - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Sus Scrofa Thymus -

CITOMIX is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Pineapple; Lenograstim; Centella Asiatica; Interferon Gamma-1b; Canakinumab; Aldesleukin; Binetrakin; Human Interleukin-6 (nonglycosylated); Sus Scrofa Small Intestine Mucosa Lymph Follicle; Sus Scrofa Bone Marrow; Cranberry; Sus Scrofa Thymus.

• Product ID: 17089-076_7d8b7d73-436a-a2cb-e053-2991aa0a3581
• NDC: 17089-076
• Product Type: Human Otc Drug
• Proprietary Name: CITOMIX
• Generic Name: Aldesleukin - Binetrakin - Canakinumab - Centella Asiatica - Cranberry - Human Interleukin-6 (nonglycosylated) - Interferon Gamma-1b - Lenograstim - Pineapple - Sus Scrofa Bone Marrow - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Sus Scrofa Thymus -
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2006-05-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: PINEAPPLE; LENOGRASTIM; CENTELLA ASIATICA; INTERFERON GAMMA-1B; CANAKINUMAB; ALDESLEUKIN; BINETRAKIN; HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED); SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE; SUS SCROFA BONE MARROW; CRANBERRY; SUS SCROFA THYMUS
• Active Ingredient Strength: 3 [hp_X]/4g; [hp_C]/4g; [hp_X]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_X]/4g; [hp_C]/4g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-076-20

2 TUBE in 1 BOX (17089-076-20) > 4 g in 1 TUBE

• Marketing Start Date: 2006-05-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-076-20 [17089007620]

CITOMIX PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-05-23
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
PINEAPPLE	3 [hp_X]/4g

OpenFDA Data

• SPL SET ID: 23886c49-5992-4a59-af52-e24eb3c9fbc5
• Manufacturer:
  • Guna spa
• UNII:
  • VP2CN2G7Y8
  • 6WS4C399GB
  • 7B69B0BD62
  • 751635Z921
  • 21K6M2I7AG
  • M89N0Q7EQR
  • 7M867G6T1U
  • 2A88ZO081O
  • 308LM01C72
  • 37CQ2C7X93
  • 0MVO31Q3QS
  • 92QVL9080Y