NDC 63479-1312 M12 Brain
Argentum Metallicum,Artemisia Vulgaris,Cicuta Virosa,Cobaltum Metallicum,Cocculus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63479 - Apex Energetics Inc
- 63479-1312 - M12
Product Packages
NDC Code 63479-1312-1
Package Description: 60 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 63479-1312?
What are the uses for M12 Brain?
What are M12 Brain Active Ingredients?
- ANAMIRTA COCCULUS SEED 4 [hp_X]/mL
- ARTEMISIA VULGARIS ROOT 2 [hp_X]/mL
- CICUTA VIROSA ROOT 6 [hp_X]/mL
- COBALT 20 [hp_X]/mL - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
- CONIUM MACULATUM FLOWERING TOP 10 [hp_X]/mL
- GINKGO 2 [hp_X]/mL
- LATHYRUS SATIVAS SEED 2 [hp_X]/mL
- LEAD 20 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
- MERCURIUS SOLUBILIS 10 [hp_Q]/mL
- POTASSIUM BROMIDE 8 [hp_X]/mL
- SALIX ALBA BARK 2 [hp_X]/mL
- SCOPOLAMINE HYDROBROMIDE 10 [hp_X]/mL
- SEQUOIADENDRON GIGANTEUM WHOLE 2 [hp_X]/mL
- SILVER 15 [hp_X]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
- STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/mL
- SUS SCROFA CEREBRUM 12 [hp_C]/mL
Which are M12 Brain UNII Codes?
The UNII codes for the active ingredients in this product are:
- SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
- SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)
- SEQUOIADENDRON GIGANTEUM WHOLE (UNII: 6CO90XQD9O)
- SEQUOIADENDRON GIGANTEUM WHOLE (UNII: 6CO90XQD9O) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (Active Moiety)
- CICUTA VIROSA ROOT (UNII: YEA9P21S8N)
- CICUTA VIROSA ROOT (UNII: YEA9P21S8N) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- COBALT (UNII: 3G0H8C9362)
- COBALT (UNII: 3G0H8C9362) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- LATHYRUS SATIVAS SEED (UNII: 8VP54WOT4I)
- LATHYRUS SATIVAS SEED (UNII: 8VP54WOT4I) (Active Moiety)
Which are M12 Brain 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 M12 Brain?
- Allergens - [CS]
- Allergens - [CS]
- Anticholinergic - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Cholinergic Antagonists - [MoA] (Mechanism of Action)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Standardized Chemical Allergen - [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".