NDC 81484-101 Detox Foot Patch

Phyllostachys Edulis Vinegar(bamboo Vinegar),Pyroligneous Acid(wood Vinegar),Schorl - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
81484-101
Proprietary Name:
Detox Foot Patch
Non-Proprietary Name: [1]
Phyllostachys Edulis Vinegar(bamboo Vinegar), Pyroligneous Acid(wood Vinegar), Schorl Tourmaline, Houttuynia Cordata Thunb
Substance Name: [2]
Houttuynia Cordata Whole; Phyllostachys Edulis Vinegar; Pyroligneous Acid; Schorl Tourmaline
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]
    Anhui Miao De Tang Pharmaceutical Co., Ltd.
    Labeler Code:
    81484
    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]
    01-29-2021
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Packages

    NDC Code 81484-101-01

    Package Description: 20 PATCH in 1 BOX

    NDC Code 81484-101-02

    Package Description: 2 PATCH in 1 BAG

    NDC Code 81484-101-03

    Package Description: 10 PATCH in 1 BAG

    Product Details

    What is NDC 81484-101?

    The NDC code 81484-101 is assigned by the FDA to the product Detox Foot Patch which is a human over the counter drug product labeled by Anhui Miao De Tang Pharmaceutical Co., Ltd.. The generic name of Detox Foot Patch is phyllostachys edulis vinegar(bamboo vinegar), pyroligneous acid(wood vinegar), schorl tourmaline, houttuynia cordata thunb. The product's dosage form is patch and is administered via topical form. The product is distributed in 3 packages with assigned NDC codes 81484-101-01 20 patch in 1 box , 81484-101-02 2 patch in 1 bag , 81484-101-03 10 patch in 1 bag . 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 Detox Foot Patch?

    Clean your feet well.Take out the patch, peel off the release paper of the adhesive patch.Place the patch in the middle of the adhesive patch(The soft side without words contact the skin.)Plase the patch on the foot and other uncomfortable parts of the body, each patch for 6-8 hours.Peel off the patch after using, wash your fee well.

    What are Detox Foot 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 Detox Foot Patch UNII Codes?

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

    Which are Detox Foot 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:

    * 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".