NDC 43857-0600 Occuloplex I
Euphrasia Officinalis,Ginkgo Biloba,Taraxacum Officinale,Hydrastis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0600 - Occuloplex
Product Packages
NDC Code 43857-0600-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0600?
What are the uses for Occuloplex I?
What are Occuloplex I Active Ingredients?
- AMMONIUM CHLORIDE 12 [hp_X]/mL - An acidifying agent that has expectorant and diuretic effects. Also used in etching and batteries and as a flux in electroplating.
- BETA CAROTENE 9 [hp_C]/mL - A carotenoid that is a precursor of VITAMIN A. Beta carotene is administered to reduce the severity of photosensitivity reactions in patients with erythropoietic protoporphyria (PORPHYRIA, ERYTHROPOIETIC).
- CALCIUM FLUORIDE 12 [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)
- CAUSTICUM 12 [hp_X]/mL
- CITRUS BIOFLAVONOIDS 8 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- CYANOCOBALAMIN 12 [hp_X]/mL
- EUPHRASIA STRICTA 3 [hp_X]/mL
- GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
- GINKGO 3 [hp_X]/mL
- GLUTATHIONE 6 [hp_X]/mL - A tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.
- GOLDENSEAL 5 [hp_X]/mL
- MAGNESIUM CARBONATE 12 [hp_X]/mL
- SELENIUM DIOXIDE 12 [hp_X]/mL - Inorganic compounds formed through the oxidation of selenium.
- SILICON DIOXIDE 12 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SUS SCROFA EYE 8 [hp_X]/mL
- TARAXACUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- UBIDECARENONE 6 [hp_X]/mL
- ZINC GLUCONATE 6 [hp_X]/mL
Which are Occuloplex I UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- HESPERIDIN (UNII: E750O06Y6O) (Active Moiety)
- SUS SCROFA EYE (UNII: X3AOK514E6)
- SUS SCROFA EYE (UNII: X3AOK514E6) (Active Moiety)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- SELENIUM DIOXIDE (UNII: 9N3UK29E57)
- SELENIUM DIOXIDE (UNII: 9N3UK29E57) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- BETA CAROTENE (UNII: 01YAE03M7J)
- BETA CAROTENE (UNII: 01YAE03M7J) (Active Moiety)
Which are Occuloplex I 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 Occuloplex I?
* 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".