NDC 17089-237 Guna-react
Angelica Sinensis Root - Arnica Montana - Asian Ginseng - Echinacea Angustifolia - - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 17089-237?
What are the uses for Guna-react?
What are Guna-react Active Ingredients?
- ANGELICA SINENSIS ROOT 3 [hp_X]/4g
- ARNICA MONTANA 4 [hp_X]/4g
- ASIAN GINSENG 1 [hp_X]/4g
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/4g - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- FOMITOPSIS PINICOLA FRUITING BODY 8 [hp_X]/4g
- INTERFERON GAMMA-1B 4 [hp_C]/4g
- PAEONIA OFFICINALIS ROOT 3 [hp_X]/4g
- PORK LIVER 4 [hp_C]/4g
- 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.
- SILYBUM MARIANUM SEED 3 [hp_X]/4g
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE 4 [hp_C]/4g
- TURMERIC 3 [hp_X]/4g
Which are Guna-react UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG)
- INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (Active Moiety)
- REISHI (UNII: TKD8LH0X2Z)
- REISHI (UNII: TKD8LH0X2Z) (Active Moiety)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72) (Active Moiety)
- PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P)
- PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P) (Active Moiety)
- FOMITOPSIS PINICOLA FRUITING BODY (UNII: 30D02U2IRN)
- FOMITOPSIS PINICOLA FRUITING BODY (UNII: 30D02U2IRN) (Active Moiety)
- TURMERIC (UNII: 856YO1Z64F)
- TURMERIC (UNII: 856YO1Z64F) (Active Moiety)
Which are Guna-react 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 Guna-react?
* 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".