Detox Foot Patchs

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

Anhui Miao De Tang Pharmaceutical Co., Ltd.
Human Otc Drug
NDC 81484-101

Detox Foot Patchs also known as Phyllostachys Edulis Vinegar(bamboo Vinegar), Pyroligneous Acid(wood Vinegar), Schorl Tourmaline, Houttuynia Cordata Thunb is a human otc drug labeled by 'Anhui Miao De Tang Pharmaceutical Co., Ltd.'. National Drug Code (NDC) number for Detox Foot Patchs is 81484-101. This drug is available in dosage form of Patch. The names of the active, medicinal ingredients in Detox Foot Patchs drug includes Houttuynia Cordata Whole - .7875 g/1 Phyllostachys Edulis Vinegar - 2.625 g/1 Pyroligneous Acid - 1.75 g/1 Schorl Tourmaline - .2625 g/1 . The currest status of Detox Foot Patchs drug is Active.

Drug Information:

Drug NDC:	81484-101
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:	Detox Foot Patchs
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:	Phyllostachys Edulis Vinegar(bamboo Vinegar), Pyroligneous Acid(wood Vinegar), Schorl Tourmaline, Houttuynia Cordata Thunb
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Anhui Miao De Tang Pharmaceutical Co., Ltd.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Patch
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:	HOUTTUYNIA CORDATA WHOLE - .7875 g/1 PHYLLOSTACHYS EDULIS VINEGAR - 2.625 g/1 PYROLIGNEOUS ACID - 1.75 g/1 SCHORL TOURMALINE - .2625 g/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
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:	29 Jan, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 Jun, 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:	Anhui Miao De Tang Pharmaceutical 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:	O3E12ZLW5T MR94DK8ZSM N4G9GAT76C 173O8XLY6T
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
81484-101-01	20 PATCH in 1 BOX (81484-101-01)	29 Jan, 2021	N/A	No
81484-101-02	2 PATCH in 1 BAG (81484-101-02)	29 Jan, 2021	N/A	No
81484-101-03	10 PATCH in 1 BAG (81484-101-03)	29 Jan, 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.

Other medicines with the same generic name

Detox Foot Patchs

Phyllostachys Edulis Vinegar(bamboo Vinegar) & more..

Patch
Anhui Miao De Tang Pharmaceutical Co., Ltd.
NDC: 81484-101

Purpose:

Purpose detox foot patchs

Product Elements:

Detox foot patchs phyllostachys edulis vinegar(bamboo vinegar), pyroligneous acid(wood vinegar), schorl tourmaline, houttuynia cordata thunb houttuynia cordata whole houttuynia cordata whole polyethylene glycol, unspecified ascorbic acid pyroligneous acid pyroligneous acid chitin schorl tourmaline schorl tourmaline phyllostachys edulis vinegar phyllostachys edulis vinegar eriobotrya japonica leaf dextrin palmitate (corn; 20000 mw)

Indications and Usage:

Use detox foot patchs to help promote sleep, relieve fatigue.

Warnings:

Warnings for external use only.

Do Not Use:

Warnings for external use only.

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.

Dosage and Administration:

Directions 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.

Stop Use:

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

Package Label Principal Display Panel:

Package label - principal display panel label

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.