NDC 63479-0302 C02 Fibrozolve
Apis Mellifica,Aurum Muriaticum Natronatum,Berberis Vulgaris,Bos Taurus Pituitarum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63479 - Apex Energetics Inc.
- 63479-0302 - C02
Product Packages
NDC Code 63479-0302-1
Package Description: 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 63479-0302?
What are the uses for C02 Fibrozolve?
What are C02 Fibrozolve Active Ingredients?
- ALLYLTHIOUREA 30 [hp_X]/mL
- APIS MELLIFERA 30 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 30 [hp_X]/mL
- BOS TAURUS PITUITARY GLAND, POSTERIOR 7 [hp_C]/mL
- CALCIUM FLUORIDE 15 [hp_X]/mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
- CALCIUM HEXAFLUOROSILICATE 30 [hp_X]/mL
- CALCIUM IODIDE 12 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 15 [hp_X]/mL
- FRAXINUS AMERICANA BARK 2 [hp_X]/mL
- GOLDENSEAL 1 [hp_X]/mL
- HYDROFLUORIC ACID 15 [hp_X]/mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
- LACTIC ACID, L- 200 [hp_X]/mL
- PANCRELIPASE 7 [hp_C]/mL - A preparation of hog pancreatic enzymes standardized for lipase content.
- SEPIA OFFICINALIS JUICE 15 [hp_X]/mL
- SODIUM TETRACHLOROAURATE 30 [hp_X]/mL
- SULFUR IODIDE 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_X]/mL
- THYROID, UNSPECIFIED 7 [hp_C]/mL
Which are C02 Fibrozolve UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3) (Active Moiety)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- ALLYLTHIOUREA (UNII: 706IDJ14B7)
- ALLYLTHIOUREA (UNII: 706IDJ14B7) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- PANCRELIPASE (UNII: FQ3DRG0N5K)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299)
- TETRACHLOROAURATE ION (UNII: ZNL6IP5PJX) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
- CALCIUM IODIDE (UNII: 8EKI9QEE2H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
Which are C02 Fibrozolve 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)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes for C02 Fibrozolve?
- Allergens - [CS]
- Bee Venoms - [CS]
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Standardized Insect Venom 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".