NDC 58264-0112 D-106
Betaine Hydrochloride,Bos Taurus Bile,Pancrelipase Lipase,Beef Liver,Sodium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0112 - D-106
Product Packages
NDC Code 58264-0112-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0112?
What are the uses for D-106?
What are D-106 Active Ingredients?
- BEEF LIVER 6 [hp_X]/mL
- BETAINE HYDROCHLORIDE 3 [hp_X]/mL - A naturally occurring compound that has been of interest for its role in osmoregulation. As a drug, betaine hydrochloride has been used as a source of hydrochloric acid in the treatment of hypochlorhydria. Betaine has also been used in the treatment of liver disorders, for hyperkalemia, for homocystinuria, and for gastrointestinal disturbances. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1341)
- BOS TAURUS BILE 6 [hp_X]/mL
- BOS TAURUS PANCREAS 6 [hp_X]/mL
- PANCRELIPASE LIPASE 3 [hp_X]/mL
- PEPSIN 3 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X]/mL
- SUS SCROFA STOMACH 6 [hp_X]/mL
Which are D-106 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETAINE HYDROCHLORIDE (UNII: JK8U8K4D6K)
- BETAINE (UNII: 3SCV180C9W) (Active Moiety)
- BOS TAURUS BILE (UNII: ET3651ZLOU)
- BOS TAURUS BILE (UNII: ET3651ZLOU) (Active Moiety)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D) (Active Moiety)
- PEPSIN (UNII: GID333S43J)
- PEPSIN (UNII: GID333S43J) (Active Moiety)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A) (Active Moiety)
Which are D-106 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)
Which are the Pharmacologic Classes for D-106?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Meat Proteins - [EXT]
- Methylating Activity - [MoA] (Mechanism of Action)
- Methylating Agent - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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".