| Drug NDC: | 44911-0659 |
| 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: | Spinapar |
| 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: | Aesculus Hippocastanum, Harpagophytum, Phytolacca Decandra, Ruta Graveolens, Cartilago Suis, Discus Intervertebralis Suis, Agaricus Muscarius, Argentum Metallicum, Arnica Montana, Bambusa Arundinacea, Bellis Perennis, Bryonia (alba), Calcarea Fluorica, Hypericum Perforatum, Rhus Tox, Sulphur, Tellurium Metallicum |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Energique, 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: | AMANITA MUSCARIA FRUITING BODY - 12 [hp_X]/mL ARNICA MONTANA WHOLE - 12 [hp_X]/mL BAMBUSA BAMBOS LEAF - 12 [hp_X]/mL BAMBUSA BAMBOS SAP - 12 [hp_X]/mL BELLIS PERENNIS WHOLE - 12 [hp_X]/mL BRYONIA ALBA ROOT - 12 [hp_X]/mL CALCIUM FLUORIDE - 12 [hp_X]/mL HARPAGOPHYTUM PROCUMBENS ROOT - 4 [hp_X]/mL HORSE CHESTNUT - 4 [hp_X]/mL HYPERICUM PERFORATUM WHOLE - 12 [hp_X]/mL Load more... PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP - 4 [hp_X]/mL SILVER - 12 [hp_X]/mL SULFUR - 12 [hp_X]/mL SUS SCROFA CARTILAGE - 6 [hp_X]/mL SUS SCROFA INTERVERTEBRAL DISC - 6 [hp_X]/mL TELLURIUM - 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF - 12 [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: | 11 Oct, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 05 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: | Energique, 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: | 0363113701760 |
| UPC stands for Universal Product Code. | |
| UNII: | DIF093I037 O80TY208ZW HW86D1FGSS DPQ0BJD6MR 2HU33I03UY T7J046YI2B O3B55K4YKI 1OYM338E89 3C18L6RJAZ XK4IUX8MNB Load more... 11E6VI8VEG N94C2U587S 3M4G523W1G 70FD1KFU70 73ECW5WG2F OJ17O2WTSM NQA0O090ZJ 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 |
|---|---|---|---|---|
| 44911-0659-1 | 30 mL in 1 BOTTLE, DROPPER (44911-0659-1) | 11 Oct, 2022 | 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.