| Drug NDC: | 63479-1403 |
| 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: | N03 Exchem |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | N03 |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | EXCHEM |
| 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: | Allium Sativum, Arsenicum Album, Benzoicum Acidum, Berberis Vulgaris, Betula Verrucosa, Calcarea Carbonica, Carbolicum Acidum, Chelidonium Majus, Chlorinum, Citricum Acidum, Histaminum, Ichthyolum, Juniperus Communis, Lycopodium Clavatum, Mercurius Solubilis, Natrum Bicarbonicum, Sodium Hypochlorite, Solidago Virgaurea, Sulphur |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Apex Energetics Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Solution/ Drops |
| 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: | ANHYDROUS CITRIC ACID - 30 [hp_X]/mL ARSENIC TRIOXIDE - 30 [hp_X]/mL BENZOIC ACID - 30 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 12 [hp_X]/mL BETULA PENDULA LEAF - 9 [hp_X]/mL CHELIDONIUM MAJUS - 9 [hp_X]/mL CHLORINE - 30 [hp_X]/mL GARLIC - 15 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE - 30 [hp_X]/mL ICHTHAMMOL - 15 [hp_X]/mL Load more... JUNIPERUS COMMUNIS STEM - 9 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 30 [hp_X]/mL MERCURIUS SOLUBILIS - 30 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 30 [hp_X]/mL PHENOL - 30 [hp_X]/mL SODIUM BICARBONATE - 30 [hp_X]/mL SODIUM HYPOCHLORITE - 30 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 9 [hp_X]/mL SULFUR - 15 [hp_X]/mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | SUBLINGUAL |
| 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, 1988 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 22 Jun, 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: | Apex Energetics 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. | |
| UPC: | 0818960012984 |
| UPC stands for Universal Product Code. | |
| NUI: | N0000175833 N0000175835 N0000175980 N0000008556 N0000175089 N0000175806 N0000175807 N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0016962 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | XF417D3PSL S7V92P67HO 8SKN0B0MIM 1TH8Q20J0U 5HW39H9KDH 7E889U5RNN 4R7X1O2820 V1V998DC17 3POA0Q644U NQ14646378 Load more... HBU87MH6OY C88X29Y479 324Y4038G2 2E32821G6I 339NCG44TV 8MDF5V39QO DY38VHM5OD 5405K23S50 70FD1KFU70 |
| 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 MOA: | Acidifying Activity [MoA] Calcium Chelating Activity [MoA] Ammonium Ion Binding Activity [MoA] |
| Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`. | |
| Pharmacologic Class EPC: | Calculi Dissolution Agent [EPC] Anti-coagulant [EPC] Nitrogen Binding Agent [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: | Decreased Coagulation Factor Activity [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] Plant 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: | Acidifying Activity [MoA] Allergens [CS] Ammonium Ion Binding Activity [MoA] Anti-coagulant [EPC] Calcium Chelating Activity [MoA] Calculi Dissolution Agent [EPC] Cell-mediated Immunity [PE] Decreased Coagulation Factor Activity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Nitrogen Binding Agent [EPC] Non-Standardized Food Allergenic Extract [EPC] Plant Proteins [CS] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 63479-1403-1 | 1 mL in 1 BOTTLE, GLASS (63479-1403-1) | 15 Jul, 1997 | 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. | ||||
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