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  4. NDC Product Code: 69176-010 Inflammation Reduction Pack

NDC 69176-010 Inflammation Reduction Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69176-010?
  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:
69176-010
Proprietary Name:
Inflammation Reduction Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tmig, Inc.
Labeler Code:
69176
Product Label ID:
f7f3dcf8-8628-467f-b195-d2dd7e11ae93
Start Marketing Date: [9]
08-18-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
9 MM
10 MM
Imprint(s):
R;550
G51;150
Score:
1

Code Structure Chart

Product Details

What is NDC 69176-010?

The NDC code 69176-010 is assigned by the FDA to the product Inflammation Reduction Pack which is product labeled by Tmig, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69176-010-01 1 kit in 1 kit , 69176-010-03 1 kit in 1 kit , 69176-010-04 1 kit in 1 kit * 60 tablet, delayed release in 1 bottle (02282-017-60) * 60 tablet in 1 bottle (68462-017-60) * 60 g in 1 tube (05912-017-60). 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.

Which are Inflammation Reduction Pack UNII Codes?

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

Which are Inflammation Reduction Pack 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 Inflammation Reduction Pack?

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:

* 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".