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  4. NDC Product Code: 53943-996 Oral Pain Relief

NDC 53943-996 Oral Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53943-996?
  4. Oral Pain Relief 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:
53943-996
Proprietary Name:
Oral Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Discount Drug Mart, Inc.
Labeler Code:
53943
Product Label ID:
242619de-ebb9-3e4d-e054-00144ff88e88
Start Marketing Date: [9]
11-09-2015
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 53943-996?

The NDC code 53943-996 is assigned by the FDA to the product Oral Pain Relief which is product labeled by Discount Drug Mart, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53943-996-42 1 tube in 1 carton / 11.9 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 Oral Pain Relief?

Directions cut open tip of tube Adults and children 2 years of age and overApply a small amount of product to the cavity and around gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or doctorChildren under 12 years of ageShould be supervised in the use of this productChildren under 2 years of ageAsk a dentist or doctor

Which are Oral Pain Relief UNII Codes?

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

Which are Oral Pain Relief 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 Oral Pain Relief?

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".