NDC 62106-1119 Unda 20
Aluminium Metallicum,Argentum Metallicum,Arsenicum Album,Aurum Metallicum,Calendula - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62106 - Seroyal Usa
- 62106-1119 - Unda 20
Product Packages
NDC Code 62106-1119-8
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 20 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 62106-1119?
What are the uses for Unda 20?
What are Unda 20 Active Ingredients?
- ALUMINUM 12 [hp_X]/20mL - A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
- ARSENIC TRIOXIDE 12 [hp_X]/20mL - 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.
- CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X]/20mL
- GOLD 12 [hp_X]/20mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
- JACARANDA CAROBA LEAF 4 [hp_X]/20mL
- JUNIPERUS SABINA LEAF 4 [hp_X]/20mL
- MARSDENIA CONDURANGO BARK 4 [hp_X]/20mL
- ROBINIA PSEUDOACACIA BARK 4 [hp_X]/20mL
- SILVER 12 [hp_X]/20mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
Which are Unda 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SARSAPARILLA (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- PRIMULA VERIS (UNII: W6LFQ57E4M)
- PRIMULA VERIS (UNII: W6LFQ57E4M) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- RHEUM TANGUTICUM WHOLE (UNII: QH89N6B02U)
- RHEUM TANGUTICUM WHOLE (UNII: QH89N6B02U) (Active Moiety)
- ENGLISH WALNUT (UNII: 1V3SHR7QB7)
- ENGLISH WALNUT (UNII: 1V3SHR7QB7) (Active Moiety)
- PILOCARPUS JABORANDI LEAF (UNII: 26ZE1BZ2US)
- PILOCARPUS JABORANDI LEAF (UNII: 26ZE1BZ2US) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II)
- THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- ALUMINUM (UNII: CPD4NFA903)
- ALUMINUM (UNII: CPD4NFA903) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA) (Active Moiety)
- JACARANDA CAROBA LEAF (UNII: AWN2M136UL)
- JACARANDA CAROBA LEAF (UNII: AWN2M136UL) (Active Moiety)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY)
- ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY) (Active Moiety)
- JUNIPERUS SABINA LEAF (UNII: 0R715588D2)
- JUNIPERUS SABINA LEAF (UNII: 0R715588D2) (Active Moiety)
Which are Unda 20 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Unda 20?
* 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".