| Drug NDC: | 17089-464 |
| 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: | Guna Flam Relief |
| 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: | Aconitum Napellus - Apis Mellifera - Arnica Montana Whole - Atropa Belladonna - Basic Cupric Carbonate - Bryonia Alba Root - Matricaria Chamomilla Whole - Calcium Sulfide - Citric Acid Monohydrate - Echinacea Angustifolia - Ferric Phosphate - Phytolacca Americana Root - Rancid Beef - Sodium Pyruvate - Pork Liver - Rancid Beef - Sus Scrofa Pituitary Gland - |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Guna Spa |
| 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: | ACONITUM NAPELLUS WHOLE - 6 [hp_X]/30mL APIS MELLIFERA - 6 [hp_X]/30mL ARNICA MONTANA - 3 [hp_X]/30mL ATROPA BELLADONNA - 6 [hp_X]/30mL BASIC CUPRIC CARBONATE - 4 [hp_X]/30mL BRYONIA ALBA ROOT - 6 [hp_X]/30mL CALCIUM SULFIDE - 6 [hp_X]/30mL CITRIC ACID MONOHYDRATE - 3 [hp_X]/30mL ECHINACEA ANGUSTIFOLIA WHOLE - 4 [hp_X]/30mL FERRIC PHOSPHATE - 12 [hp_X]/30mL Load more... MATRICARIA CHAMOMILLA WHOLE - 2 [hp_X]/30mL PHYTOLACCA AMERICANA ROOT - 6 [hp_X]/30mL PORK LIVER - 6 [hp_X]/30mL RANCID BEEF - 30 [hp_X]/30mL SODIUM PYRUVATE - 3 [hp_X]/30mL SUS SCROFA PITUITARY GLAND - 200 [hp_X]/30mL |
| 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: | 24 Sep, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 10 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: | Guna spa |
| 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: | N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | U0NQ8555JD 7S82P3R43Z O80TY208ZW WQZ3G9PF0H GIK928GH0Y T7J046YI2B 1MBW07J51Q 2968PHW8QP VB06AV5US8 N6BAA189V1 Load more... G0R4UBI2ZZ 11E6VI8VEG 6EC706HI7F 29SUH5R3HU POD38AIF08 L0PFEMQ1DT |
| 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: | Standardized Insect Venom 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] Bee Venoms [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] Anti-coagulant [EPC] Bee Venoms [CS] Calcium Chelating Activity [MoA] Calculi Dissolution Agent [EPC] Cell-mediated Immunity [PE] Decreased Coagulation Factor Activity [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Iron [CS] Parenteral Iron Replacement [EPC] Phosphate Binder [EPC] Phosphate Chelating Activity [MoA] Standardized Insect Venom 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 |
|---|---|---|---|---|
| 17089-464-18 | 1 BOTTLE, DROPPER in 1 BOX (17089-464-18) / 30 mL in 1 BOTTLE, DROPPER | 24 Sep, 2020 | 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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