| Drug NDC: | 43857-0449 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. | |
| Proprietary Name: | Occuloplex I |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | Occuloplex |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | I |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| Non Proprietary Name: | Euphrasia Officinalis, Ginkgo Biloba, Taraxacum Officinale, Hydrastis Canadensis, Beta Carotene, Cyanocobalamin, Glutathione, Ubidecarenonum, Zincum Gluconicum, Citrus Bioflavonoids, Eye (bovine), Ammonium Muriaticum, Calcarea Fluorica, Causticum, Conium Maculatum, Germanium Sesquioxide, Magnesia Carbonica, Selenium Dioxide, Silicea |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Bioactive Nutritional, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | .BETA.-CAROTENE - 6 [hp_X]/mL AMMONIUM CHLORIDE - 12 [hp_X]/mL BOS TAURUS EYE - 8 [hp_X]/mL CALCIUM CHLORIDE - 12 [hp_X]/mL CAUSTICUM - 12 [hp_X]/mL CITRUS BIOFLAVONOIDS - 8 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP - 12 [hp_X]/mL CYANOCOBALAMIN - 6 [hp_X]/mL EUPHRASIA STRICTA - 3 [hp_X]/mL GERMANIUM SESQUIOXIDE - 12 [hp_X]/mL Load more... GINKGO - 3 [hp_X]/mL GLUTATHIONE - 6 [hp_X]/mL GOLDENSEAL - 5 [hp_X]/mL MAGNESIUM CARBONATE - 12 [hp_X]/mL SELENIUM DIOXIDE - 12 [hp_X]/mL SILICON DIOXIDE - 12 [hp_X]/mL TARAXACUM OFFICINALE - 3 [hp_X]/mL UBIDECARENONE - 6 [hp_X]/mL ZINC - 6 [hp_X]/mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. | |
| Marketing Start Date: | 08 Jun, 2017 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 17 Oct, 2023 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. | |
| Listing Expiration Date: | 09 May, 2026 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | BioActive Nutritional, Inc. |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| NUI: | M0022794 N0000175951 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | 01Q9PC255D VTW461N43P M4I0D6VV5M DD5FO1WKFU BD70459I50 Q28R5GF371 P6YC3EG204 C9642I91WL 96WE91N25T 19FUJ2C58T Load more... GAN16C9B8O ZW3Z11D0JV 0E53J927NA 9N3UK29E57 ETJ7Z6XBU4 39981FM375 EJ27X76M46 J41CSQ7QDS |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Pharmacologic Class EPC: | Vitamin B12 [EPC] |
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. | |
| Pharmacologic Class CS: | Vitamin B 12 [CS] |
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. | |
| Pharmacologic Class: | Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Increased Coagulation Factor Activity [PE] Vitamin B 12 [CS] Vitamin B12 [EPC] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 43857-0449-1 | 30 mL in 1 BOTTLE, DROPPER (43857-0449-1) | 08 Jun, 2017 | 17 Oct, 2023 | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
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