NDC 62106-1113 Unda 14
Eucalyptus Globulus,Inula Helenium,Jateorhiza Palmata,Camphora,Argentum Metallicum,Aurum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62106 - Seroyal Usa
- 62106-1113 - Unda 14
Product Packages
NDC Code 62106-1113-8
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 20 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 62106-1113?
What are the uses for Unda 14?
What are Unda 14 Active Ingredients?
- CAMPHOR (NATURAL) 4 [hp_X]/20mL
- COPPER 12 [hp_X]/20mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- EUCALYPTUS GLOBULUS LEAF 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.
- INULA HELENIUM ROOT 4 [hp_X]/20mL
- JATEORHIZA CALUMBA ROOT 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 14 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (Active Moiety)
- MERCURIALIS PERENNIS (UNII: Q35465A1MA)
- MERCURIALIS PERENNIS (UNII: Q35465A1MA) (Active Moiety)
- CRATAEGUS FRUIT (UNII: Q21UUL2105)
- CRATAEGUS FRUIT (UNII: Q21UUL2105) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) (Active Moiety)
- CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59)
- CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59) (Active Moiety)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- POTENTILLA ERECTA ROOT (UNII: BI896CKT6B)
- POTENTILLA ERECTA ROOT (UNII: BI896CKT6B) (Active Moiety)
- ADIANTUM CAPILLUS-VENERIS LEAF (UNII: 4817H7M565)
- ADIANTUM CAPILLUS-VENERIS LEAF (UNII: 4817H7M565) (Active Moiety)
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG)
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
- GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
- INULA HELENIUM ROOT (UNII: E55SMD6DA8)
- INULA HELENIUM ROOT (UNII: E55SMD6DA8) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- TUSSILAGO FARFARA WHOLE (UNII: 6177A89GA2)
- TUSSILAGO FARFARA WHOLE (UNII: 6177A89GA2) (Active Moiety)
- JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5)
- JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
Which are Unda 14 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 14?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [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".