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  4. NDC Product Code: 83702-015 Xinhuazhx Lymphatic Detox Patch

NDC 83702-015 Xinhuazhx Lymphatic Detox Patch

Aconitum,Arsenic Iodide,Honeysuckle Patch Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83702-015?
  4. Xinhuazhx Lymphatic Detox Patch Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
83702-015
Proprietary Name:
Xinhuazhx Lymphatic Detox Patch
Non-Proprietary Name: [1]
Aconitum, Arsenic Iodide, Honeysuckle
Substance Name: [2]
Aconitum Chasmanthum Whole; Arsenic Triiodide; Lonicera Caprifolium Flower
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
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]
    Puning Xinhua Trade Co., Ltd.
    Labeler Code:
    83702
    Product Label ID:
    08096e84-4053-75ed-e063-6294a90a9c25
    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]
    06-01-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83702-015?

    The NDC code 83702-015 is assigned by the FDA to the product Xinhuazhx Lymphatic Detox Patch which is a human over the counter drug product labeled by Puning Xinhua Trade Co., Ltd.. The generic name of Xinhuazhx Lymphatic Detox Patch is aconitum, arsenic iodide, honeysuckle. The product's dosage form is patch and is administered via topical form. The product is distributed in a single package with assigned NDC code 83702-015-12 6 patch in 1 bag / 2.1 g in 1 patch (83702-015-11). 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 Xinhuazhx Lymphatic Detox Patch?

    Use to Support the detoxification of organs and the discharge of lymph glands. Temporarily alleviate discomfort caused by lymphatic swelling and edema, repair lymph nodes, cleanse and enhance immunity

    What are Xinhuazhx Lymphatic Detox Patch 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.

    Which are Xinhuazhx Lymphatic Detox Patch UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
    • LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) (Active Moiety)
    • ACONITUM CHASMANTHUM WHOLE (UNII: 9R0ETE1IDH)
    • ACONITUM CHASMANTHUM WHOLE (UNII: 9R0ETE1IDH) (Active Moiety)
    • ARSENIC TRIIODIDE (UNII: 3029988O2T)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)

    Which are Xinhuazhx Lymphatic Detox Patch Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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    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".