NDC 62106-1135 Unda 36
Aconitum Napellus,Aesculus Hippocastanum,Aluminium Metallicum,Chelidonium Majus,Hamamelis - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62106-1135?
What are the uses for Unda 36?
What are Unda 36 Active Ingredients?
- ACONITUM NAPELLUS 4 [hp_X]/20mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
- ALUMINUM 12 [hp_X]/20mL - A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
- CHELIDONIUM MAJUS ROOT 4 [hp_X]/20mL
- GOLDENSEAL 4 [hp_X]/20mL
- HAMAMELIS VIRGINIANA BARK 4 [hp_X]/20mL
- HORSE CHESTNUT 4 [hp_X]/20mL - A plant genus of the family HIPPOCASTANACEAE (or SAPINDACEAE by some) that contains antimicrobial protein 1 and escin. A. hippocastanum is used in folk medicine for treating chronic venous insufficiency.
- HYPERICUM PERFORATUM 4 [hp_X]/20mL
Which are Unda 36 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- ALUMINUM (UNII: CPD4NFA903)
- ALUMINUM (UNII: CPD4NFA903) (Active Moiety)
- CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N)
- CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (Active Moiety)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
Which are Unda 36 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)
* 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".