NDC 83027-0126 Detox Liquescence
Chelidonium Majus,Echinacea (angustifolia),Juniperus Communis,Rhamnus Purshiana,Stigmata - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0126?
What are the uses for Detox Liquescence?
What are Detox Liquescence Active Ingredients?
- ARCTOSTAPHYLOS UVA-URSI LEAF 3 [hp_X]/mL
- BEEF KIDNEY 6 [hp_X]/mL
- BEEF LIVER 6 [hp_X]/mL
- BOS TAURUS GALLBLADDER 6 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 3 [hp_X]/mL
- CORN SILK 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- FRANGULA PURSHIANA BARK 3 [hp_X]/mL
- GALIUM APARINE WHOLE 6 [hp_X]/mL
- JUNIPER BERRY 3 [hp_X]/mL
- LAMB 6 [hp_X]/mL
- RUMEX CRISPUS ROOT 6 [hp_X]/mL
- SMILAX ORNATA ROOT 4 [hp_X]/mL
- SUS SCROFA LYMPH 8 [hp_X]/mL
- SUS SCROFA URINARY BLADDER 6 [hp_X]/mL
- TARAXACUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
Which are Detox Liquescence UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- JUNIPER BERRY (UNII: O84B5194RL)
- JUNIPER BERRY (UNII: O84B5194RL) (Active Moiety)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F)
- FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F) (Active Moiety)
- CORN SILK (UNII: 7D3VB244UX)
- CORN SILK (UNII: 7D3VB244UX) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- GALIUM APARINE WHOLE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- BOS TAURUS GALLBLADDER (UNII: 9901V1E867)
- BOS TAURUS GALLBLADDER (UNII: 9901V1E867) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- LAMB (UNII: FOF26T73HA)
- LAMB (UNII: FOF26T73HA) (Active Moiety)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
Which are Detox 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)
Which are the Pharmacologic Classes for Detox Liquescence?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Meat Proteins - [EXT]
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* 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".