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  4. NDC Product Code: 72982-1903 Turmeric Pain Relieving Cream

NDC 72982-1903 Turmeric Pain Relieving Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72982-1903?
  4. Turmeric Pain Relieving 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:
72982-1903
Proprietary Name:
Turmeric Pain Relieving Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Everyday Medical Llc
Labeler Code:
72982
Product Label ID:
8695e3ec-619d-f2e4-e053-2a91aa0a15b0
Start Marketing Date: [9]
04-08-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 72982-1903?

The NDC code 72982-1903 is assigned by the FDA to the product Turmeric Pain Relieving Cream which is product labeled by Everyday Medical Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72982-1903-1 141 g in 1 container . 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 Turmeric Pain Relieving Cream?

Temporarily relieves minor pain associated witharthritissimple backachemuscle strainsbruisessprainscramps

Which are Turmeric Pain Relieving Cream UNII Codes?

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

Which are Turmeric Pain Relieving 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".