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  4. NDC Product Code: 82093-002 Diolpure Lidocaine Pain Relief Cream

NDC 82093-002 Diolpure Lidocaine Pain Relief Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82093-002?
  4. Diolpure Lidocaine Pain Relief Cream Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82093-002
Proprietary Name:
Diolpure Lidocaine Pain Relief Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Diolpure, Llc
Labeler Code:
82093
Product Label ID:
c6b3df6f-f18e-7a5f-e053-2995a90a96b4
Start Marketing Date: [9]
07-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82093-002?

The NDC code 82093-002 is assigned by the FDA to the product Diolpure Lidocaine Pain Relief Cream which is product labeled by Diolpure, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82093-002-01 1 bottle, pump in 1 carton / 56.7 g in 1 bottle, pump. 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 Diolpure Lidocaine Pain Relief Cream?

Adults and children 12 years of age and older: Apply to affected area every 6 to 8 hours, do not exceed 3 to 4 applications in a 24 hour period Before and after applying, wash hands with soap and waterChildren under 12 years of age: Consult a doctor

Which are Diolpure Lidocaine Pain Relief Cream UNII Codes?

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

Which are Diolpure Lidocaine Pain Relief Cream 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".