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  4. NDC Product Code: 83050-251 Lanlijen Menthol Pain Relief

NDC 83050-251 Lanlijen Menthol Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83050-251?
  4. Lanlijen Menthol Pain Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
83050-251
Proprietary Name:
Lanlijen Menthol Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Chaben Medical Healthcare Technology Co.,ltd
Labeler Code:
83050
Product Label ID:
efb5af5e-b7e6-19d1-e053-2a95a90a88b4
Start Marketing Date: [9]
12-15-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 83050-251?

The NDC code 83050-251 is assigned by the FDA to the product Lanlijen Menthol Pain Relief which is product labeled by Jiangsu Chaben Medical Healthcare Technology Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83050-251-05 5 patch in 1 box / 9 g in 1 patch (83050-251-01). 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 Lanlijen Menthol Pain Relief?

Adults and children 12 years of age and older, Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. Clean and dry afected areas, partially peel back protective film and apply exposed patch to site of pain. Children under 12 years of age, Consult physician

Which are Lanlijen Menthol Pain Relief UNII Codes?

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

Which are Lanlijen Menthol 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 Lanlijen Menthol 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:

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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".