NDC 57955-2817 Skin Irritations And Itch Relief
Agaricus Muscarius,Alumina,Anagallis Arvensis,Antimonium Tartaricum,Apis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-2817 - Skin Irritations And Itch Relief
Product Packages
NDC Code 57955-2817-2
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-2817?
What are the uses for Skin Irritations And Itch Relief?
What are Skin Irritations And Itch Relief Active Ingredients?
- ALUMINUM OXIDE 10 [hp_X]/59mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
- AMANITA MUSCARIA FRUITING BODY 10 [hp_X]/59mL
- ANTIMONY POTASSIUM TARTRATE 10 [hp_X]/59mL - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- APIS MELLIFERA 10 [hp_X]/59mL
- ARSENIC TRIIODIDE 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.
- CAUSTICUM 10 [hp_X]/59mL
- FAGOPYRUM ESCULENTUM WHOLE 10 [hp_X]/59mL
- GRAPHITE 10 [hp_X]/59mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- HYDROCHLORIC ACID 10 [hp_X]/59mL - A strong corrosive acid that is commonly used as a laboratory reagent. It is formed by dissolving hydrogen chloride in water. GASTRIC ACID is the hydrochloric acid component of GASTRIC JUICE.
- KEROSENE 10 [hp_X]/59mL - A refined petroleum fraction used as a fuel as well as a solvent.
- LYCOPERDON UTRIFORME FRUITING BODY 10 [hp_X]/59mL
- LYSIMACHIA ARVENSIS WHOLE 10 [hp_X]/59mL
- MUCUNA PRURIENS FRUIT TRICHOME 10 [hp_X]/59mL
- NERIUM OLEANDER LEAF 10 [hp_X]/59mL
- PINE TAR 10 [hp_X]/59mL
- POTASSIUM CHLORIDE 10 [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.
- RADIUM BROMIDE 12 [hp_X]/59mL
- SELENIUM 10 [hp_X]/59mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
- 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.
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/59mL
- URTICA URENS WHOLE 10 [hp_X]/59mL
Which are Skin Irritations And Itch Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- LYSIMACHIA ARVENSIS WHOLE (UNII: 46883LR90E)
- ANAGALLIS ARVENSIS EXTRACT (UNII: 46883LR90E) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C) (Active Moiety)
- FAGOPYRUM ESCULENTUM WHOLE (UNII: B10M69172N)
- FAGOPYRUM ESCULENTUM (UNII: B10M69172N) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYDROCHLORIC ACID (UNII: QTT17582CB) (Active Moiety)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- PINE TAR (UNII: YFH4WC535J)
- PINE TAR (UNII: YFH4WC535J) (Active Moiety)
- RADIUM BROMIDE (UNII: R74O7T8569)
- RADIUM CATION (UNII: 05456MVL7T) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
Which are Skin Irritations And Itch 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 Skin Irritations And Itch Relief?
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [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".