| Drug NDC: | 17089-067 |
| 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: | Anti Age Stress |
| 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: | Acetylcysteine - Ballota Foetida - Epinephrine - Glutathione - Interferon Gamma-1b - Lenograstim - Lithium Carbonate - Melatonin - Penicillium Glabrum - Potassium Carbonate - Pummelo - Rhodotorula Rubra - Silver Nitrate - Strychnos Nux-vomica Seed - Sus Scrofa Cerebral Cortex - Sus Scrofa Stomach - Sus Scrofa Superior Gastric Plexus - Sus Scrofa Thalamus - |
| 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: | Pellet |
| 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: | ACETYLCYSTEINE - 4 [hp_C]/4g BALLOTA FOETIDA - 3 [hp_X]/4g EPINEPHRINE - 9 [hp_C]/4g GLUTATHIONE - 4 [hp_C]/4g INTERFERON GAMMA-1B - 5 [hp_C]/4g LENOGRASTIM - 4 [hp_C]/4g LITHIUM CARBONATE - 8 [hp_X]/4g MELATONIN - 15 [hp_C]/4g PENICILLIUM GLABRUM - 8 [hp_X]/4g POTASSIUM CARBONATE - 9 [hp_C]/4g Load more... PUMMELO - 3 [hp_X]/4g RHODOTORULA RUBRA - 8 [hp_X]/4g SILVER NITRATE - 9 [hp_C]/4g STRYCHNOS NUX-VOMICA SEED - 5 [hp_C]/4g SUS SCROFA CEREBRAL CORTEX - 4 [hp_C]/4g SUS SCROFA STOMACH - 7 [hp_C]/4g SUS SCROFA SUPERIOR GASTRIC PLEXUS - 7 [hp_C]/4g SUS SCROFA THALAMUS - 7 [hp_C]/4g |
| 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: | 23 May, 2006 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 14 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: | N0000175429 N0000175961 N0000008867 N0000175960 N0000175776 N0000175547 N0000000209 N0000000245 N0000175552 N0000175555 N0000175570 M0003647 N0000175541 M0011490 N0000185372 N0000175629 N0000184306 N0000185001 M0008890 M0000728 N0000185375 M0016962 M0516536 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | WYQ7N0BPYC YKH834O4BH GAN16C9B8O 21K6M2I7AG 6WS4C399GB 2BMD2GNA4V JL5DK93RCL 2IN23YUE0I BQN1B9B9HA ET1TN5W71X Load more... 15W81V867R 95IT3W8JZE 269XH13919 538Q433GB7 T0920P9Z9A F4679CEE8H 3D6Q7UV74J |
| 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: | Reduction Activity [MoA] Adrenergic alpha-Agonists [MoA] Adrenergic beta-Agonists [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: | Antidote [EPC] Antidote for Acetaminophen Overdose [EPC] Mucolytic [EPC] alpha-Adrenergic Agonist [EPC] beta-Adrenergic Agonist [EPC] Catecholamine [EPC] Interferon gamma [EPC] Non-Standardized Fungal 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: | Decreased Respiratory Secretion Viscosity [PE] Increased Glutathione Concentration [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: | Catecholamines [CS] Interferon-gamma [CS] Fungal Proteins [CS] Allergens [CS] Plant 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: | Adrenergic alpha-Agonists [MoA] Adrenergic beta-Agonists [MoA] Allergens [CS] Antidote [EPC] Antidote for Acetaminophen Overdose [EPC] Catecholamine [EPC] Catecholamines [CS] Cell-mediated Immunity [PE] Decreased Respiratory Secretion Viscosity [PE] Fungal Proteins [CS] Increased Glutathione Concentration [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Interferon gamma [EPC] Interferon-gamma [CS] Mood Stabilizer [EPC] Mucolytic [EPC] Non-Standardized Fungal Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Reduction Activity [MoA] Seed Storage Proteins [CS] alpha-Adrenergic Agonist [EPC] beta-Adrenergic Agonist [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 |
|---|---|---|---|---|
| 17089-067-20 | 2 TUBE in 1 BOX (17089-067-20) / 4 g in 1 TUBE | 21 Dec, 2018 | 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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