NDC 72624-001 Chinese Medicine Patch

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72624-001
Proprietary Name:
Chinese Medicine Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hubei Lishizhen Modern Biological Medicine Group Co.,ltd.
Labeler Code:
72624
Start Marketing Date: [9]
12-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72624-001-01

Package Description: 2 BAG in 1 BOX / 3 PACKAGE in 1 BAG / 240 mL in 1 PACKAGE

Product Details

What is NDC 72624-001?

The NDC code 72624-001 is assigned by the FDA to the product Chinese Medicine Patch which is product labeled by Hubei Lishizhen Modern Biological Medicine Group Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72624-001-01 2 bag in 1 box / 3 package in 1 bag / 240 ml in 1 package. 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 Chinese Medicine Patch?

Pain relief, hot release, warming uterus, hemostatic, can be used to improve the conditioning neck, back, hands and feet and other rheumatism pain and spleen and stomach caused by cold injury, deficiency diarrhea and other conditions.Apply one paster on stomach venter.

Which are Chinese Medicine Patch UNII Codes?

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

Which are Chinese Medicine 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

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

[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".