Cozaco Woman
Red Ginseng
Kone Bio Logics Co., Ltd.
Human Otc Drug
NDC 81651-0002Cozaco Woman also known as Red Ginseng is a human otc drug labeled by 'Kone Bio Logics Co., Ltd.'. National Drug Code (NDC) number for Cozaco Woman is 81651-0002. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Cozaco Woman drug includes Panax Ginseng Root Oil - 44.2 1/1 . The currest status of Cozaco Woman drug is Active.
Drug Information:
| Drug NDC: | 81651-0002 |
| 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: | Cozaco Woman |
| 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: | Red Ginseng |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Kone Bio Logics Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Tablet |
| 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: | PANAX GINSENG ROOT OIL - 44.2 1/1
|
| 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 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: | 10 Mar, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 04 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. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Kone Bio Logics 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. |
| UNII: | P9T4K47OM0
|
| 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. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 81651-0002-1 | 100 TABLET in 1 BOTTLE (81651-0002-1) | 10 Mar, 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 blood circulation, antioxidant effect, memory improvement, fatigue improvement, boost immunity, urinary incontinence
Product Elements:
Cozaco woman red ginseng garlic oil panax ginseng root oil panax ginseng root oil
Indications and Usage:
Indication & usage section take 2 tablets a day (after having dinner, before sleep)
Warnings:
Warning please check product ingredients if you have any allergies before taking. please be careful during open the product package. keep product out of direct sunlight, high temperature and humidity. store in a cool dry place. any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item. consult your doctor if any abnormal symptoms occur
Dosage and Administration:
Uses for oral use only
Package Label Principal Display Panel:
Label