NDC 58264-0210 N-12
Phosphoric Acid,Cinchona Officinalis Bark,Anemone Pulsatilla,Phosphorus,Picric - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58264 - Dna Labs, Inc.
- 58264-0210 - N-12
Product Packages
NDC Code 58264-0210-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 58264-0210?
What are the uses for N-12?
What are N-12 Active Ingredients?
- ANEMONE PULSATILLA 6 [hp_X]/mL
- BOS TAURUS ADRENAL GLAND 200 [hp_X]/mL
- BOS TAURUS OVARY 200 [hp_X]/mL
- BOS TAURUS PITUITARY GLAND, POSTERIOR 200 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 6 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/mL
- PHOSPHORIC ACID 6 [hp_X]/mL
- PHOSPHORUS 6 [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.
- PICRIC ACID 6 [hp_X]/mL
- THYROID, UNSPECIFIED 200 [hp_X]/mL
- VIBURNUM OPULUS WHOLE 2 [hp_X]/mL
Which are N-12 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PICRIC ACID (UNII: A49OS0F91S)
- PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- VIBURNUM OPULUS WHOLE (UNII: DIO510WJ04)
- VIBURNUM OPULUS WHOLE (UNII: DIO510WJ04) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
- BOS TAURUS OVARY (UNII: 66LZN1C747)
- BOS TAURUS OVARY (UNII: 66LZN1C747) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
Which are N-12 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 N-12?
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- 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)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".