NDC 57955-2833 Restless Leg Symptom Relief
Arsenicum Album,Bufo Rana,Causticum,Chamomilla,Crotalus Horridus,Digitalis - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-2833?
What are the uses for Restless Leg Symptom Relief?
What are Restless Leg Symptom Relief Active Ingredients?
- 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.
- BUFO BUFO CUTANEOUS GLAND 10 [hp_X]/59mL
- CAUSTICUM 10 [hp_X]/59mL
- CROTALUS HORRIDUS HORRIDUS VENOM 10 [hp_X]/59mL
- DIGITALIS 10 [hp_X]/59mL - A genus of toxic herbaceous Eurasian plants of the Plantaginaceae which yield cardiotonic DIGITALIS GLYCOSIDES. The most useful species are Digitalis lanata and D. purpurea.
- LACHESIS MUTA VENOM 10 [hp_X]/59mL
- LILIUM LANCIFOLIUM WHOLE FLOWERING 10 [hp_X]/59mL
- LYCOSA TARANTULA 10 [hp_X]/59mL
- MATRICARIA CHAMOMILLA WHOLE 10 [hp_X]/59mL
- PULSATILLA VULGARIS WHOLE 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.
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/59mL
- VISCUM ALBUM FRUITING TOP 10 [hp_X]/59mL
- ZINC 10 [hp_X]/59mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
Which are Restless Leg Symptom Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (Active Moiety)
- DIGITALIS (UNII: F1T8QT9U8B)
- DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
- LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
- PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- LYCOSA TARANTULA (UNII: 86M454L2TT)
- LYCOSA TARANTULA (UNII: 86M454L2TT) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
Which are Restless Leg Symptom 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)
* 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".