NDC 57955-9002 Allergy Hay Fever Reliever
Allium Cepa,Ambrosia Artemisiaefolia,Arsenicum Album,Arum Triphyllum,Arundo - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-9002 - Allergy Hay Fever Reliever
Product Packages
NDC Code 57955-9002-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-9002?
What are the uses for Allergy Hay Fever Reliever?
What are Allergy Hay Fever Reliever Active Ingredients?
- AMBROSIA ARTEMISIIFOLIA WHOLE 10 [hp_X]/59mL
- ARISAEMA TRIPHYLLUM ROOT 10 [hp_X]/59mL
- ARSENIC TRIOXIDE 10 [hp_X]/59mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- ARUNDO PLINIANA ROOT 10 [hp_X]/59mL
- EUPHRASIA STRICTA 10 [hp_X]/59mL
- NAPHTHALENE 10 [hp_X]/59mL
- ONION 10 [hp_X]/59mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- SCHOENOCAULON OFFICINALE SEED 10 [hp_X]/59mL
- SODIUM CHLORIDE 10 [hp_X]/59mL - A ubiquitous sodium salt that is commonly used to season food.
- WYETHIA HELENIOIDES ROOT 10 [hp_X]/59mL
Which are Allergy Hay Fever Reliever UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (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)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- NAPHTHALENE (UNII: 2166IN72UN)
- NAPHTHALENE (UNII: 2166IN72UN) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
Which are Allergy Hay Fever Reliever 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 Allergy Hay Fever Reliever?
* 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".