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  4. NDC Product Code: 83872-998 Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng

NDC 83872-998 Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng

Gieng Compound Capsulens Capsule Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83872-998?
  4. Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng Uses
  5. Active Ingredients

Product Information

NDC Product Code:
83872-998
Proprietary Name:
Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng
Non-Proprietary Name: [1]
Gieng Compound Capsulens
Substance Name: [2]
Asian Ginseng
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Shenzhen Xiaomai Manufacturing Co., Ltd.
    Labeler Code:
    83872
    Product Label ID:
    0ec042e5-fa67-4bf5-e063-6394a90a76f3
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    01-14-2024
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83872-998?

    The NDC code 83872-998 is assigned by the FDA to the product Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng which is a human over the counter drug product labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. The generic name of Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng is gieng compound capsulens. The product's dosage form is capsule and is administered via topical form. The product is distributed in a single package with assigned NDC code 83872-998-01 15250 mg in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng?

    Take two capsules daily, orally

    What are Niwedah Shilajit Ashwagandha Rhodiola Rosea Panaxginseng Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".