| Drug NDC: | 64578-0143 |
| 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: | Vac-chord |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| 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: | Alumina, Arsenicum Album, Baptisia Tinctoria, Belladonna, Boldo, Calcarea Carbonica, Carduus Marianus, Chamomilla, Chelidonium Majus, Echinacea, Hydrastis Canadensis, Lecithin, Ledum Palustre, Lycopodium Clavatum, Mercurius Solubilis, Morbillinum, Pertussinum, Phytolacca Decandra, Pyrogenium, Rhus Tox, Silicea, Sulphur, Taraxacum Officinale, Thuja Occidentalis, Thyroidinum. |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Energetix Corporation |
| 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: | ALUMINUM OXIDE - 15 [hp_X]/59.1mL ARSENIC TRIOXIDE - 12 [hp_X]/59.1mL ATROPA BELLADONNA - 12 [hp_X]/59.1mL BAPTISIA TINCTORIA ROOT - 4 [hp_X]/59.1mL CHELIDONIUM MAJUS - 4 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/59.1mL EGG PHOSPHOLIPIDS - 12 [hp_X]/59.1mL GOLDENSEAL - 5 [hp_X]/59.1mL HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - 30 [hp_X]/59.1mL LEDUM PALUSTRE TWIG - 16 [hp_X]/59.1mL Load more... LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/59.1mL MATRICARIA RECUTITA - 12 [hp_X]/59.1mL MEASLES VIRUS - 30 [hp_X]/59.1mL MERCURIUS SOLUBILIS - 15 [hp_X]/59.1mL MILK THISTLE - 4 [hp_X]/59.1mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 12 [hp_X]/59.1mL PEUMUS BOLDUS LEAF - 4 [hp_X]/59.1mL PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/59.1mL RANCID BEEF - 30 [hp_X]/59.1mL SILICON DIOXIDE - 12 [hp_X]/59.1mL SULFUR - 15 [hp_X]/59.1mL TARAXACUM OFFICINALE - 4 [hp_X]/59.1mL THUJA OCCIDENTALIS LEAFY TWIG - 6 [hp_X]/59.1mL THYROID, UNSPECIFIED - 9 [hp_X]/59.1mL TOXICODENDRON PUBESCENS LEAF - 12 [hp_X]/59.1mL |
| 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: | 22 Sep, 2017 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 09 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: | Energetix Corporation |
| 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: | 0364578022315 |
| UPC stands for Universal Product Code. | |
| UNII: | LMI26O6933 S7V92P67HO WQZ3G9PF0H 5EF0HWI5WU 7E889U5RNN VB06AV5US8 1Z74184RGV ZW3Z11D0JV U364V64HUN 877L01IZ0P Load more... C88X29Y479 G0R4UBI2ZZ HT3R7C012Q 324Y4038G2 U946SH95EE 2E32821G6I Q4EWM09M3O 11E6VI8VEG 29SUH5R3HU ETJ7Z6XBU4 70FD1KFU70 39981FM375 1NT28V9397 0B4FDL9I6P 6IO182RP7A |
| 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. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 64578-0143-1 | 59.1 mL in 1 BOTTLE, DROPPER (64578-0143-1) | 22 Sep, 2017 | 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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