NDC 17089-465 Guna Pain Management
Achillea Millefolium Whole - Bellis Perennis Whole - Matricaria Chamomilla Whole - - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-465 - Guna Pain Management
Product Packages
NDC Code 17089-465-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-465?
What are the uses for Guna Pain Management?
What are Guna Pain Management Active Ingredients?
- ACHILLEA MILLEFOLIUM WHOLE 2 [hp_X]/30mL
- APIS MELLIFERA 30 [hp_X]/30mL
- ARNICA MONTANA WHOLE 3 [hp_X]/30mL
- BELLIS PERENNIS WHOLE 2 [hp_X]/30mL
- BRYONIA ALBA ROOT 6 [hp_X]/30mL
- COMFREY ROOT 6 [hp_X]/30mL
- HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/30mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
- HYPERICUM PERFORATUM 3 [hp_X]/30mL
- KALMIA LATIFOLIA LEAF 6 [hp_X]/30mL
- MATRICARIA CHAMOMILLA WHOLE 2 [hp_X]/30mL
- PORK LIVER 6 [hp_X]/30mL
- RUTA GRAVEOLENS FLOWERING TOP 4 [hp_X]/30mL
- TOXICODENDRON PUBESCENS LEAF 8 [hp_X]/30mL
Which are Guna Pain Management UNII Codes?
The UNII codes for the active ingredients in this product are:
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- BELLIS PERENNIS WHOLE (UNII: 2HU33I03UY)
- BELLIS PERENNIS WHOLE (UNII: 2HU33I03UY) (Active Moiety)
- MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
Which are Guna Pain Management 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:
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Guna Pain Management?
* 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".