| Drug NDC: | 63479-0602 |
| 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: | F02 Angr-flx |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | F02 |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | ANGR-FLX |
| 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: | Adelheid Aqua, Arsenicum Album, Big Sagebrush, Bos Taurus Liver, Gallbladder, Briza Maxima, Calendula Officinalis, Cayenne, Chamomile , Chicory , Garlic, English Holly , European Beech , Forking Larkspur , German Chamomile , Impatiens Glandulifera , Juglans Regia , Lilium Tigrinum, Morning Glory, Mountain Dogwood, Natrum Muriaticum, Nux Vomica, Pinus Sylvestris , Redwood, Rubber Rabbitbrush, Sepia, Tolmie Star Tulip, Verbena Officinalis , Vitis Vinifera , Watermelon, White Willow , Yellow Star Thistle |
| 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: | ALLIUM SATIVUM WHOLE - 12 [hp_C]/mL ARSENIC TRIOXIDE - 15 [hp_C]/mL ARTEMISIA TRIDENTATA WHOLE - 12 [hp_C]/mL BEEF LIVER - 60 [hp_C]/mL BOS TAURUS GALLBLADDER - 60 [hp_C]/mL BRIZA MAXIMA WHOLE - 12 [hp_C]/mL CALENDULA OFFICINALIS FLOWERING TOP - 12 [hp_C]/mL CALOCHORTUS TOLMIEI WHOLE - 12 [hp_C]/mL CAPSICUM - 12 [hp_C]/mL CENTAUREA SOLSTITIALIS WHOLE - 12 [hp_C]/mL Load more... CHAMOMILE - 12 [hp_C]/mL CICHORIUM INTYBUS FLOWER - 12 [hp_C]/mL CONSOLIDA REGALIS FLOWER - 12 [hp_C]/mL CORNUS NUTTALLII WHOLE - 12 [hp_C]/mL ERICAMERIA NAUSEOSA WHOLE - 12 [hp_C]/mL FAGUS SYLVATICA FLOWERING TOP - 12 [hp_C]/mL ILEX AQUIFOLIUM FLOWERING TOP - 12 [hp_C]/mL IMPATIENS GLANDULIFERA FLOWER - 12 [hp_C]/mL IPOMOEA PURPUREA TOP - 12 [hp_C]/mL JUGLANS REGIA FLOWERING TOP - 12 [hp_C]/mL LILIUM LANCIFOLIUM WHOLE FLOWERING - 12 [hp_C]/mL MATRICARIA CHAMOMILLA FLOWERING TOP - 12 [hp_C]/mL PINUS SYLVESTRIS FLOWERING TOP - 12 [hp_C]/mL SALIX ALBA FLOWERING TOP - 12 [hp_C]/mL SEPIA OFFICINALIS JUICE - 15 [hp_C]/mL SEQUOIA SEMPERVIRENS WHOLE - 12 [hp_C]/mL SODIUM CHLORIDE - 12 [hp_C]/mL STRYCHNOS NUX-VOMICA SEED - 20 [hp_X]/mL VERBENA OFFICINALIS FLOWERING TOP - 12 [hp_C]/mL VITIS VINIFERA FLOWERING TOP - 12 [hp_C]/mL WATER - 12 [hp_C]/mL WATERMELON - 12 [hp_C]/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: | 12 Mar, 1996 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 06 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: | 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: | 0818960011765 |
| UPC stands for Universal Product Code. | |
| NUI: | N0000185371 N0000175629 N0000184306 M0000728 M0006342 N0000185017 N0000185375 M0016962 M0022575 N0000185001 M0516536 N0000185015 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | IIF21WT8O3 S7V92P67HO 45E08M336T W8N8R55022 9901V1E867 3SU44U90RR 18E7415PXQ 831MXG026J 00UK7646FG 59CH355QGQ Load more... FGL3685T2X HW54500A89 3O33B2269R F34859WS62 H52XVP0BVB 21AF0IHY5U 5ENR9SAN1W AJU5O1A5ZV XMQ0V9812O 3BA2N709NG X67Z2963PI 3VNC7T6Z02 2HEM73YI9I XBP5X7E70R QDL83WN8C2 AH099J2PN6 451W47IQ8X 269XH13919 311PNK9CDZ 6TG3V35HTV 059QF0KO0R 231473QB6R |
| 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] Non-Standardized Plant 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] Increased IgG Production [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] Vegetable Proteins [CS] Seed Storage 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] Dietary Proteins [CS] Fruit Proteins [EXT] Increased Histamine Release [PE] Increased IgG Production [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Meat Proteins [EXT] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Plant Proteins [CS] Seed Storage Proteins [CS] Vegetable 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 |
|---|---|---|---|---|
| 63479-0602-1 | 30 mL in 1 BOTTLE, GLASS (63479-0602-1) | 12 Mar, 1996 | 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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