NDC 81484-101 Detox Foot Patchs

Phyllostachys Edulis Vinegar(bamboo Vinegar), Pyroligneous Acid(wood Vinegar), Schorl Tourmaline, Houttuynia Cordata Thunb

NDC Product Code 81484-101

NDC CODE: 81484-101

Proprietary Name: Detox Foot Patchs What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Phyllostachys Edulis Vinegar(bamboo Vinegar), Pyroligneous Acid(wood Vinegar), Schorl Tourmaline, Houttuynia Cordata Thunb 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.

NDC Code Structure

NDC 81484-101-01

Package Description: 20 PATCH in 1 BOX

NDC 81484-101-02

Package Description: 2 PATCH in 1 BAG

NDC Product Information

Detox Foot Patchs with NDC 81484-101 is a a human over the counter drug product labeled by Anhui Miao De Tang Pharmaceutical Co., Ltd.. The generic name of Detox Foot Patchs 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.

Labeler Name: Anhui Miao De Tang Pharmaceutical Co., Ltd.

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’.

Product Type: Human Otc Drug 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.

Detox Foot Patchs Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Anhui Miao De Tang Pharmaceutical Co., Ltd.
Labeler Code: 81484
Marketing Category: UNAPPROVED DRUG OTHER - 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.

Start Marketing Date: 01-29-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Detox Foot Patchs Product Label Images

Detox Foot Patchs Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index


Detox Foot Patch

Active Ingredient(S)

PHYLLOSTACHYS EDULIS VINEGAR(Bamboo vinegar) 2.625g/patch

Pyroligneous acid(wood vinegar) 1.75g/patch


Houttuynia cordata thunb 0.7875g/patch


Detox Foot Patchs


Detox Foot Patchs to help promote sleep, relieve fatigue.


For external use only.

Do Not Use

  • In children less than 12 years of ageon open skin wounds

Otc - When Using

Do not use otherwise than directed.Do not stretch out the adhesive tape.Do not take out the contents from the patch.If patch is damaged, discard it right away. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.Keep out of reach of children.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


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.

Other Information

  • Sealed, keep in cool place.

Inactive Ingredients


Loquat leaf



Vitamin C

* Please review the disclaimer below.