Dermall Matrix Quick Vitalizing
Adenosine
Dermall Matrix Co., Ltd.
Human Otc Drug
NDC 82428-010Dermall Matrix Quick Vitalizing also known as Adenosine is a human otc drug labeled by 'Dermall Matrix Co., Ltd.'. National Drug Code (NDC) number for Dermall Matrix Quick Vitalizing is 82428-010. This drug is available in dosage form of Patch. The names of the active, medicinal ingredients in Dermall Matrix Quick Vitalizing drug includes Adenosine - .04 g/100g . The currest status of Dermall Matrix Quick Vitalizing drug is Active.
Drug Information:
| Drug NDC: | 82428-010 |
| 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: | Dermall Matrix Quick Vitalizing |
| 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: | Adenosine |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Dermall Matrix Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Patch |
| 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: | ADENOSINE - .04 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| 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 Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED DRUG OTHER |
| 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: | 01 Dec, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 2025 |
| 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. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Dermall Matrix Co., Ltd.
|
| 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: | N0000178375
N0000175788
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | K72T3FS567
|
| 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: | Adenosine Receptor 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: | Adenosine Receptor Agonist [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: | Adenosine Receptor Agonist [EPC]
Adenosine Receptor Agonists [MoA]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 82428-010-02 | 10 PATCH in 1 CARTON (82428-010-02) / 6 g in 1 PATCH (82428-010-01) | 01 Dec, 2021 | 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. |
Purpose:
Purpose anti wrinkle
Product Elements:
Dermall matrix quick vitalizing adenosine adenosine adenosine water glycerin calcium chloride
Indications and Usage:
Uses helps improve wrinkles to disappear.
Warnings:
Warnings 1. avoid using on blemishes, pimples, irritated or sunburned skin 2. avoid using on skin which is sensitive to bandages, tapes or peel-off masks. 3. stop using if skin becomes reddish, swollen or itchy, during and after usage. 4. avoid contact with eyes directly. 5. for external use only. keep out of reach of children. 6. avoid severe stimulation when you attach biogel sheets. 7. once opened, use biogel sheet immediately.
Dosage and Administration:
Directions 1. choose areas that require quick moisturizing and calming. 2. take off the plastic cover on both sides after opening aluminum pouch. 3. attach biogel sheet to desired area. 4. the longer the use, the thinner the biogel sheets.
Package Label Principal Display Panel:
Package label.principal display panel image of carton
Further Questions:
Questions www.dermallmatrix.com +82-70-4115-7665