NDC 83027-0037 Degex Liquescence
Thuja Occidentalis,Ubidecarenonum,Conium Maculatum,Asterias Rubens,Germanium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0037?
What are the uses for Degex Liquescence?
What are Degex Liquescence Active Ingredients?
- ASTERIAS RUBENS 12 [hp_X]/mL
- BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 9 [hp_X]/mL
- GERMANIUM 12 [hp_X]/mL - A rare metal element with a blue-gray appearance and atomic symbol Ge, atomic number 32, and atomic weight 72.63.
- HUMAN BREAST TUMOR CELL 16 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
- UBIDECARENONE 8 [hp_X]/mL
Which are Degex Liquescence UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- ASTERIAS RUBENS (UNII: A7FYY9Q742)
- ASTERIAS RUBENS (UNII: A7FYY9Q742) (Active Moiety)
- GERMANIUM (UNII: 00072J7XWS)
- GERMANIUM (UNII: 00072J7XWS) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
Which are Degex Liquescence 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".