NDC 83027-0052 Blood Liquescence
Allium Cepa,Hyssopus Officinalis,Avena Sativa,Paloondo,Urtica Dioica,Trifolium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0052?
What are the uses for Blood Liquescence?
What are Blood Liquescence Active Ingredients?
- AVENA SATIVA FLOWERING TOP 2 [hp_X]/mL
- BOS TAURUS SPLEEN 6 [hp_X]/mL
- CAMPHOR (NATURAL) 8 [hp_X]/mL
- CAPSICUM 6 [hp_X]/mL - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
- GINGER 3 [hp_X]/mL
- HYSSOPUS OFFICINALIS FLOWERING TOP 1 [hp_X]/mL
- JUGLANS REGIA LEAF 6 [hp_X]/mL
- LARREA TRIDENTATA LEAF 2 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/mL
- ONION 1 [hp_X]/mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PORK LIVER 6 [hp_X]/mL
- RANCID BEEF 20 [hp_X]/mL
- RUMEX CRISPUS ROOT 6 [hp_X]/mL
- SUS SCROFA BONE MARROW 6 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
- URTICA DIOICA WHOLE 2 [hp_X]/mL
Which are Blood Liquescence UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- HYSSOPUS OFFICINALIS FLOWERING TOP (UNII: X7HKN4FOJI)
- HYSSOPUS OFFICINALIS FLOWERING TOP (UNII: X7HKN4FOJI) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P) (Active Moiety)
- URTICA DIOICA WHOLE (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
Which are Blood 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 Blood Liquescence?
- Allergens - [CS]
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
- Vegetable 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".