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  4. NDC Product Code: 11673-345 Pain Relieving

NDC 11673-345 Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11673-345?
  4. Pain Relieving 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:
11673-345
Proprietary Name:
Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Product Label ID:
83ff36dd-9be4-190b-e053-2a91aa0a7ac6
Start Marketing Date: [9]
03-13-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 11673-345?

The NDC code 11673-345 is assigned by the FDA to the product Pain Relieving which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11673-345-60 60 patch in 1 box / 1 patch in 1 patch. 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 Relieving?

Directionsadults and children 12 years of age and older:clean and dry affected arearemove patch from filmapply to affected area no more than 3 to 4 times dailydo not water patch for more than 8 hourschildren under 12 years of age: consult a doctor

Which are Pain Relieving UNII Codes?

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

Which are Pain Relieving 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".