NDC 17089-076 Citomix
Aldesleukin - Binetrakin - Canakinumab - Centella Asiatica - Cranberry - Human Interleukin...

Product Information

What is NDC 17089-076?

The NDC code 17089-076 is assigned by the FDA to the product Citomix which is a human over the counter drug product labeled by Guna Spa. The generic name of Citomix is 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 -. The product's dosage form is pellet and is administered via oral form. The product is distributed in a single package with assigned NDC code 17089-076-20 2 tube in 1 box / 4 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code17089-076
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Citomix
Non-Proprietary Name 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.		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 -
Product Type 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.		Human Otc Drug
Dosage FormPellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Guna Spa
Labeler Code17089
Marketing Category 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.		UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		05-23-2006
Listing Expiration Date 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.		12-31-2023
Exclude Flag 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". 		N
NDC Code Structure

What are the uses for Citomix?


Product Characteristics

Color(s)WHITE (C48325 - WHITE)

Product Packages

NDC Code 17089-076-20

Package Description: 2 TUBE in 1 BOX / 4 g in 1 TUBE

Product Details

What are Citomix Active Ingredients?

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.

Citomix Active Ingredients UNII Codes

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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Citomix Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients/Purpose



ANANASSA    3X        IMMUNE SUPPORT
GCSF          4C, 9C, 15C, 30C    IMMUNE SUPPORT
HYDROCOTYLE ASIATICA    3X    INFLAMMATION
INTERFERON GAMMA    4C    IMMUNE SUPPORT
INTERLEUKIN  1 BETA    5C    IMMUNE SUPPORT
INTERLEUKIN 2     5C, 7C        FEVER REDUCER
INTERLEUKIN 4    4C        FEVER REDUCER
INTERLEUKIN 6     7C, 9C, 15C    IMMUNE SUPPORT
LYMPHATIC  VESSEL    4C    DETOXIFICATION
MEDULLA OSSIS        4C    DETOXIFICATION
MOUNTAIN CRANBERRY    3X    DECONGESTION
THYMUS GLAND         4C    IMMUNE SUPPORT


Uses



For Immune Support during times of seasonal colds and flu


Warnings



Stop use and ask doctor if cold and flu-like symptoms such as fever, sore throat, headache, minor aches and pain worsen or persist more than 5 days

Keep this and all medicines out of reach of children


Pregnancy



If pregnant or breast-feeding ask a health professional before use.


Directions



Take 15 minutes before meals
Adults and children 12 years and older    5 pellets 3 times per day
Children between 12 years and 6 years of age   3 pellets 3 times per day
Children under 6 years     1 pellet 3 times per day to be dissolved into a little water


Questions



Questions?: [email protected]
tel. (484) 223-3500


* Please review the disclaimer below.