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  4. NDC Product Code: 10237-747 Orajel Instant Pain Relief Severe

NDC 10237-747 Orajel Instant Pain Relief Severe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10237-747?
  4. Orajel Instant Pain Relief Severe 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:
10237-747
Proprietary Name:
Orajel Instant Pain Relief Severe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Church Dwight Co., Inc.
Labeler Code:
10237
Product Label ID:
4ce932f7-46fd-2caf-e054-00144ff88e88
Start Marketing Date: [9]
02-27-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10237-747-32

Package Description: 1 TUBE in 1 CARTON / 9.4 g in 1 TUBE

Product Details

What is NDC 10237-747?

The NDC code 10237-747 is assigned by the FDA to the product Orajel Instant Pain Relief Severe which is product labeled by Church Dwight Co., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10237-747-32 1 tube in 1 carton / 9.4 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 Orajel Instant Pain Relief Severe?

This product is used as Oral pain relieverOral Pain relieverAntiseptic

Which are Orajel Instant Pain Relief Severe UNII Codes?

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

Which are Orajel Instant Pain Relief Severe 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 Orajel Instant Pain Relief Severe?

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:
  • RxCUI: 1483194 - benzalkonium chloride 0.1 % / benzocaine 20 % / menthol 0.25 % Topical Cream
  • RxCUI: 1483194 - benzalkonium chloride 1 MG/ML / benzocaine 200 MG/ML / menthol 2.5 MG/ML Topical Cream

* 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".