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  4. NDC Product Code: 82075-410 Pain Relief Cream

NDC 82075-410 Pain Relief Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82075-410?
  4. Pain Relief Cream 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:
82075-410
Proprietary Name:
Pain Relief Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sagely Enterprises Inc.
Labeler Code:
82075
Product Label ID:
c624fa53-c565-9114-e053-2a95a90acca3
Start Marketing Date: [9]
07-02-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82075-410-10

Package Description: 1 BOTTLE, PUMP in 1 CARTON / 118 g in 1 BOTTLE, PUMP

NDC Code 82075-410-95

Package Description: 1 TUBE in 1 CARTON / 88 g in 1 TUBE

Product Details

What is NDC 82075-410?

The NDC code 82075-410 is assigned by the FDA to the product Pain Relief Cream which is product labeled by Sagely Enterprises Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82075-410-10 1 bottle, pump in 1 carton / 118 g in 1 bottle, pump, 82075-410-95 1 tube in 1 carton / 88 g in 1 tube. 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 Pain Relief Cream?

Use only as directedAdults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily Children under 12 years of age: ask a doctor

Which are Pain Relief Cream UNII Codes?

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

Which are 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:

What is the NDC to RxNorm Crosswalk for Pain Relief Cream?

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".