NDC 61821-052 Dieda Fengshi Gao Medicated

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:
61821-052
Proprietary Name:
Dieda Fengshi Gao Medicated
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
61821
Start Marketing Date: [9]
06-17-2013
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 61821-052?

The NDC code 61821-052 is assigned by the FDA to the product Dieda Fengshi Gao Medicated which is product labeled by Guangzhou Baiyunshan Jingxiutang Pharmaceutical Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61821-052-01 5 plaster in 1 box . 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 Dieda Fengshi Gao Medicated?

UsesFor the temporary relief of minor aches and pains of muscles and jointsdue to: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Which are Dieda Fengshi Gao Medicated UNII Codes?

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

Which are Dieda Fengshi Gao Medicated 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:

What is the NDC to RxNorm Crosswalk for Dieda Fengshi Gao Medicated?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1429374 - camphor 8.3 % / menthol 3.32 % / methyl salicylate 13.84 % Medicated Patch
  • RxCUI: 1429374 - camphor 0.083 MG/MG / menthol 0.0332 MG/MG / methyl salicylate 0.138 MG/MG Medicated Patch

* Please review the disclaimer below.

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".