NDC 57955-0762 Regional Allergies Southern U.s.
Adenosinum Cyclophosphoricum,Adrenalinum,Adrenocorticotrophin,Allium Cepa,Alnus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 57955-0762?
What are the uses for Regional Allergies Southern U.s.?
What are Regional Allergies Southern U.s. Active Ingredients?
- ADENOSINE CYCLIC PHOSPHATE 12 [hp_X]/59mL
- ALNUS SERRULATA BARK 12 [hp_X]/59mL
- ARISAEMA TRIPHYLLUM ROOT 12 [hp_X]/59mL
- ARUNDO PLINIANA ROOT 12 [hp_X]/59mL
- CENTAUREA BENEDICTA 12 [hp_X]/59mL - A plant species of the genus CENTAUREA and family ASTERACEAE. Members contain sesquiterpene lactone CNICIN.
- CHICORY ROOT 12 [hp_X]/59mL
- CORTICOTROPIN 30 [hp_X]/59mL
- CORTISONE ACETATE 12 [hp_X]/59mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
- EPINEPHRINE 12 [hp_X]/59mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
- EUPHRASIA STRICTA 12 [hp_X]/59mL
- GALPHIMIA GLAUCA FLOWERING TOP 12 [hp_X]/59mL
- HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/59mL - 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.
- JUGLANS CINEREA BRANCH BARK/ROOT BARK 12 [hp_X]/59mL
- MUCUNA PRURIENS FRUIT TRICHOME 12 [hp_X]/59mL
- NASTURTIUM OFFICINALE 12 [hp_X]/59mL - A plant genus of the family BRASSICACEAE. Nasturtium is also used as a common name for TROPAEOLUM. The common name of watercress is also used for RORIPPA & TROPAEOLUM. This is the most popular of the edible cresses, is a hardy creeping perennial plant, native to Europe but extensively naturalized elsewhere in moist places.
- ONION 12 [hp_X]/59mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- POTASSIUM CHLORIDE 12 [hp_X]/59mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
- SACCHAROMYCES CEREVISIAE RNA 12 [hp_X]/59mL
- SASSAFRAS ALBIDUM ROOT BARK 12 [hp_X]/59mL
- SCHOENOCAULON OFFICINALE SEED 12 [hp_X]/59mL
- SODIUM CHLORIDE 12 [hp_X]/59mL - A ubiquitous sodium salt that is commonly used to season food.
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/59mL
Which are Regional Allergies Southern U.s. UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- ALNUS SERRULATA BARK (UNII: BQ5P19J9OL)
- ALNUS SERRULATA BARK (UNII: BQ5P19J9OL) (Active Moiety)
- ARISAEMA TRIPHYLLUM ROOT (UNII: DM64K844DM)
- ARISAEMA TRIPHYLLUM ROOT (UNII: DM64K844DM) (Active Moiety)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
- CENTAUREA BENEDICTA (UNII: 6L5ZL09795)
- CENTAUREA BENEDICTA (UNII: 6L5ZL09795) (Active Moiety)
- CHICORY ROOT (UNII: 090CTY533N)
- CHICORY ROOT (UNII: 090CTY533N) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- JUGLANS CINEREA BRANCH BARK/ROOT BARK (UNII: 48FZ1BHO18)
- JUGLANS CINEREA BRANCH BARK/ROOT BARK (UNII: 48FZ1BHO18) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- SASSAFRAS ALBIDUM ROOT BARK (UNII: XC5UMP9I5F)
- SASSAFRAS ALBIDUM ROOT BARK (UNII: XC5UMP9I5F) (Active Moiety)
Which are Regional Allergies Southern U.s. 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 Regional Allergies Southern U.s.?
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- Allergens - [CS]
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
- Corticosteroid - [EPC] (Established Pharmacologic Class)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
* 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".