NDC 63083-9420 Thyroid Nosode Combination 9420
Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 63083-9420 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 63083-9420?
What are the uses for Thyroid Nosode Combination 9420?
What are Thyroid Nosode Combination 9420 Active Ingredients?
- CALCIUM FLUORIDE 10 [hp_X]/29.5mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
- COLCHICUM AUTUMNALE BULB 4 [hp_X]/29.5mL
- FUCUS VESICULOSUS 6 [hp_X]/29.5mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
- FUMARIC ACID 8 [hp_X]/29.5mL
- HYSSOPUS OFFICINALIS WHOLE 8 [hp_X]/29.5mL
- MALIC ACID 8 [hp_X]/29.5mL
- OXOGLURIC ACID 8 [hp_X]/29.5mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
- PULSATILLA MONTANA WHOLE 8 [hp_X]/29.5mL
- SODIUM DIETHYL OXALACETATE 8 [hp_X]/29.5mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/29.5mL
- THYROID, UNSPECIFIED 12 [hp_X]/29.5mL
Which are Thyroid Nosode Combination 9420 UNII Codes?
The UNII codes for the active ingredients in this product are:
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- OXOGLURIC ACID (UNII: 8ID597Z82X)
- OXOGLURIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- MALIC ACID (UNII: 817L1N4CKP)
- MALIC ACID (UNII: 817L1N4CKP) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
Which are Thyroid Nosode Combination 9420 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".