NDC 17089-076 Citomix
Aldesleukin - Binetrakin - Canakinumab - Centella Asiatica - Cranberry - Human - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-076 - Citomix
Product Characteristics
Product Packages
NDC Code 17089-076-20
Package Description: 2 TUBE in 1 BOX / 4 g in 1 TUBE
Product Details
What is NDC 17089-076?
What are the uses for Citomix?
What are Citomix Active Ingredients?
- ALDESLEUKIN 5 [hp_C]/4g
- BINETRAKIN 4 [hp_C]/4g
- CANAKINUMAB 5 [hp_C]/4g
- CENTELLA ASIATICA 3 [hp_X]/4g - A plant of the family APIACEAE which is the source of asiatic acid and asiaticoside. Centella asiatica (L.) Urb. = Hydrocotyle asiatica L. is known for effect on peripheral circulation.
- CRANBERRY 3 [hp_X]/4g
- HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) 7 [hp_C]/4g
- INTERFERON GAMMA-1B 4 [hp_C]/4g
- LENOGRASTIM 4 [hp_C]/4g - A recombinant granulocyte colony-stimulating factor that is used to treat or prevent NEUTROPENIA in patients receiving myelosuppressive cancer chemotherapy, for the preparation and collection of blood progenitor cells in PERIPHERAL BLOOD STEM CELL TRANSPLANTATION; and in the treatment of severe congenital neutropenia. Component 1 and Component 2 differ by absence or presence of Neu5Ac in 2-6 linkage to GalNAc side chain.
- PINEAPPLE 3 [hp_X]/4g
- SUS SCROFA BONE MARROW 4 [hp_C]/4g
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE 4 [hp_C]/4g
- SUS SCROFA THYMUS 4 [hp_C]/4g
Which are Citomix UNII Codes?
The UNII codes for the active ingredients in this product are:
- PINEAPPLE (UNII: 2A88ZO081O)
- PINEAPPLE (UNII: 2A88ZO081O) (Active Moiety)
- LENOGRASTIM (UNII: 6WS4C399GB)
- LENOGRASTIM (UNII: 6WS4C399GB) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (Active Moiety)
- CANAKINUMAB (UNII: 37CQ2C7X93)
- CANAKINUMAB (UNII: 37CQ2C7X93) (Active Moiety)
- ALDESLEUKIN (UNII: M89N0Q7EQR)
- ALDESLEUKIN (UNII: M89N0Q7EQR) (Active Moiety)
- BINETRAKIN (UNII: 751635Z921)
- BINETRAKIN (UNII: 751635Z921) (Active Moiety)
- HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) (UNII: 92QVL9080Y)
- HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) (UNII: 92QVL9080Y) (Active Moiety)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72) (Active Moiety)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
- CRANBERRY (UNII: 0MVO31Q3QS)
- CRANBERRY (UNII: 0MVO31Q3QS) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
Which are Citomix Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SUCROSE (UNII: C151H8M554)
Which are the Pharmacologic Classes for Citomix?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Fruit Proteins - [EXT]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased Lymphocyte Activation - [PE] (Physiologic Effect)
- Increased Lymphocyte Cell Production - [PE] (Physiologic Effect)
- Interferon gamma - [EPC] (Established Pharmacologic Class)
- Interferon-gamma - [CS]
- Interleukin-2 - [CS]
- Lymphocyte Growth Factor - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".