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  4. NDC Product Code: 37205-122 Leader Oral Analgesic

NDC 37205-122 Leader Oral Analgesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37205-122?
  4. Leader Oral Analgesic 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:
37205-122
Proprietary Name:
Leader Oral Analgesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Product Label ID:
26875610-8552-4e41-a4fe-7710a4a93846
Start Marketing Date: [9]
05-01-2012
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37205-122-12

Package Description: 1 TUBE in 1 CARTON / 11.9 g in 1 TUBE

Product Details

What is NDC 37205-122?

The NDC code 37205-122 is assigned by the FDA to the product Leader Oral Analgesic which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-122-12 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 Leader Oral Analgesic?

Directionsremove cap and cut tip of tube on score markadults and children 2 years of age and older: apply a small amount of Oral Analgesic Gel to the cavity and around gum surrounding the teeth. Use up to 4 times daily or as directed by a doctor or dentistchildren under 12 years of age: should be supervised when using this productchildren under 2 years of age: ask a doctor/dentist

Which are Leader Oral Analgesic UNII Codes?

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

Which are Leader Oral Analgesic 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 Leader Oral Analgesic?

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".