NDC 70836-001 Sincere Pain Relief

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:
70836-001
Proprietary Name:
Sincere Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Jiangsu Sincere Pharmaceutical Co., Ltd
Labeler Code:
70836
Start Marketing Date: [9]
05-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70836-001-01

Package Description: 5 BAG in 1 BOX / 12 g in 1 BAG

Product Details

What is NDC 70836-001?

The NDC code 70836-001 is assigned by the FDA to the product Sincere Pain Relief which is product labeled by Jiangsu Jiangsu Sincere Pharmaceutical Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70836-001-01 5 bag in 1 box / 12 g 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 Sincere Pain Relief?

Adults and children 12 years of age and over:1. Clean and dry the affected areas.2. Peel off the protective transparent film, paste the gel surface to the affected area.3. Remove patch from the skin after at most 12 hours' application. The patch works by cold compression. You may feel cold when using.Children under 12 years of age:Consult a doctor.

Which are Sincere Pain Relief UNII Codes?

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

Which are Sincere Pain Relief 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 Sincere Pain Relief?

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: 1812745 - menthol 2 % / methyl salicylate 2 % Medicated Patch
  • RxCUI: 1812745 - menthol 0.02 MG/MG / methyl salicylate 0.02 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".