Guna-tonsils Pellet
NDC 17089-235

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 17089-235?
  5. Guna-tonsils Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

Guna-tonsils (angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen - interleukin-11 -) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Guna Spa. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a white pellet for oral administration. This product entry covers the primary NDC 17089-235 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
17089-235
Proprietary Name:
Guna-tonsils
Non-Proprietary Name: [1]
Angelica Sinensis Root - Binetrakin - Interleukin-3 - Lenograstim - Melatonin - Reishi - Shiitake Mushroom - Sus Scrofa Blood - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Sus Scrofa Spleen - Interleukin-11 -
Substance Name: [2]
Angelica Sinensis Root; Binetrakin; Interleukin-11; Interleukin-3; Lenograstim; Melatonin; Reishi; Shiitake Mushroom; Sus Scrofa Blood; Sus Scrofa Small Intestine Mucosa Lymph Follicle; Sus Scrofa Spleen
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Pellet - 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): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Guna Spa
Labeler Code:
17089
Product Label ID:
b7d0a24f-c702-4b4a-8494-a4cbbb020257
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-23-2006
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)

Code Structure Chart

Product Details

What is NDC 17089-235?

The NDC code 17089-235 is assigned by the FDA to the product Guna-tonsils. It is commonly known by its generic name, angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen - interleukin-11 -. This pharmaceutical product is labeled by Guna Spa and is currently categorized as listed product. The medication is a pellet administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 17089-235-20. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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

What are Active Ingredients of this product?

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.
  • ANGELICA SINENSIS ROOT 3 [hp_X]/4g
  • BINETRAKIN 4 [hp_C]/4g
  • INTERLEUKIN-11 5 [hp_C]/4g - A lymphohematopoietic cytokine that plays a role in regulating the proliferation of ERYTHROID PRECURSOR CELLS. It induces maturation of MEGAKARYOCYTES which results in increased production of BLOOD PLATELETS. Interleukin-11 was also initially described as an inhibitor of ADIPOGENESIS of cultured preadipocytes.
  • INTERLEUKIN-3 5 [hp_C]/4g - A multilineage cell growth factor secreted by LYMPHOCYTES; EPITHELIAL CELLS; and ASTROCYTES which stimulates clonal proliferation and differentiation of various types of blood and tissue cells.
  • 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.
  • MELATONIN 4 [hp_C]/4g - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
  • REISHI 8 [hp_X]/4g - A mushroom, Ganoderma lucidum, of the POLYPORALES order of basidiomycetous fungi. It has long been used in traditional Chinese medicine in various forms.
  • SHIITAKE MUSHROOM 8 [hp_X]/4g - Mushrooms in the order AGARICALES containing B vitamins, cortinelin, and the polysaccharide LENTINAN.
  • SUS SCROFA BLOOD 7 [hp_C]/4g
  • SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE 4 [hp_C]/4g
  • SUS SCROFA SPLEEN 4 [hp_C]/4g

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated 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:

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".