| Drug NDC: | 63083-9245 |
| 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: | Selenium Combination 9245 |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | Selenium Combination |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | 9245 |
| 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: | Selenium Combination |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Professional Complementary Health Formulas |
| 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: | AMMONIUM CATION - 12 [hp_X]/29.5mL ARCTIUM LAPPA ROOT OIL - 6 [hp_X]/29.5mL BEEF KIDNEY - 10 [hp_X]/29.5mL BEEF LIVER - 10 [hp_X]/29.5mL BOS TAURUS PLACENTA - 10 [hp_X]/29.5mL BOS TAURUS SPLEEN - 10 [hp_X]/29.5mL CALCIUM FLUORIDE - 6 [hp_X]/29.5mL CHICKEN SKIN, COOKED - 10 [hp_X]/29.5mL CORTISONE ACETATE - 28 [hp_X]/29.5mL FORMIC ACID - 198 [hp_X]/29.5mL Load more... FUMARIC ACID - 10 [hp_X]/29.5mL GALIUM APARINE WHOLE - 6 [hp_X]/29.5mL HORSE CHESTNUT - 6 [hp_X]/29.5mL MERCURIUS SOLUBILIS - 13 [hp_X]/29.5mL OXOGLURIC ACID - 10 [hp_X]/29.5mL PHOSPHORIC ACID - 6 [hp_X]/29.5mL RHODODENDRON TOMENTOSUM LEAFY TWIG - 4 [hp_X]/29.5mL SELENIUM - 10 [hp_X]/29.5mL SODIUM DIETHYL OXALACETATE - 10 [hp_X]/29.5mL STRYCHNOS IGNATII SEED - 6 [hp_X]/29.5mL SULFUR - 8 [hp_X]/29.5mL THUJA OCCIDENTALIS LEAF - 8 [hp_X]/29.5mL URTICA URENS WHOLE - 4 [hp_X]/29.5mL |
| 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: | 15 Aug, 1984 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 08 May, 2026 |
| 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: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Professional Complementary Health Formulas |
| 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: | N0000185371 N0000175629 N0000184306 M0000728 M0006342 N0000185017 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | 54S68520I4 55DGS3F5YG 5HOC10FSIC W8N8R55022 83AL37E3A7 190Q9MB3U3 O3B55K4YKI 00GG7UT6PL 883WKN7W8X 0YIW783RG1 Load more... 88XHZ13131 Z4B6561488 3C18L6RJAZ 324Y4038G2 8ID597Z82X E4GA8884NN 877L01IZ0P H6241UJ22B 6CA025Y4FG 1NM3M2487K 70FD1KFU70 0T0DQN8786 IHN2NQ5OF9 |
| 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: | Non-Standardized Food Allergenic Extract [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 PE: | Increased Histamine Release [PE] Cell-mediated Immunity [PE] |
| Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`. | |
| Pharmacologic Class CS: | Allergens [CS] Dietary Proteins [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: | Allergens [CS] Cell-mediated Immunity [PE] Corticosteroid Hormone Receptor Agonists [MoA] Corticosteroid [EPC] Dietary Proteins [CS] Increased Histamine Release [PE] Meat Proteins [EXT] Non-Standardized Food Allergenic Extract [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 |
|---|---|---|---|---|
| 63083-9245-1 | 29.5 mL in 1 BOTTLE, DROPPER (63083-9245-1) | 15 Aug, 1985 | N/A | 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. | ||||
* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.