NDC 57955-2845 Migraine Relief
Gelsemium Sempervirens,Glonoinum,Iris Versicolor,Kali Carbonicum,Lycopodium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-2845 - Migraine Relief
Product Packages
NDC Code 57955-2845-2
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-2845?
What are the uses for Migraine Relief?
What are Migraine Relief Active Ingredients?
- CLAVICEPS PURPUREA SCLEROTIUM 10 [hp_X]/59mL
- GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/59mL
- IRIS VERSICOLOR ROOT 10 [hp_X]/59mL
- LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/59mL
- NICKEL 10 [hp_X]/59mL - A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.
- NITROGLYCERIN 10 [hp_X]/59mL - A volatile vasodilator which relieves ANGINA PECTORIS by stimulating GUANYLATE CYCLASE and lowering cytosolic calcium. It is also sometimes used for TOCOLYSIS and explosives.
- POTASSIUM CARBONATE 10 [hp_X]/59mL
- SANGUINARIA CANADENSIS ROOT 10 [hp_X]/59mL
- SODIUM CHLORIDE 10 [hp_X]/59mL - A ubiquitous sodium salt that is commonly used to season food.
- SPIGELIA ANTHELMIA WHOLE 10 [hp_X]/59mL
- STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/59mL
- SULFUR 10 [hp_X]/59mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
Which are Migraine Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- NICKEL (UNII: 7OV03QG267)
- NICKEL (UNII: 7OV03QG267) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Migraine Relief 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- ORANGE PEEL (UNII: TI9T76XD44)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY)
- CARYA OVATA BARK (UNII: X765CF609L)
- STEVIOL (UNII: 4741LYX6RT)
Which are the Pharmacologic Classes for Migraine Relief?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nitrate Vasodilator - [EPC] (Established Pharmacologic Class)
- Nitrates - [CS]
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Vasodilation - [PE] (Physiologic Effect)
* 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".