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  4. NDC Product Code: 53045-125 Opahl

NDC 53045-125 Opahl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53045-125?
  5. Opahl Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
53045-125
Proprietary Name:
Opahl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dharma Research, Inc.
Labeler Code:
53045
Product Label ID:
2b4a6b21-396a-4b07-b1b9-751643cb5821
Start Marketing Date: [9]
01-01-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
SPEARMINT (C73416)

Code Structure Chart

Product Details

What is NDC 53045-125?

The NDC code 53045-125 is assigned by the FDA to the product Opahl which is product labeled by Dharma Research, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53045-125-60 60 g in 1 bottle . 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 Opahl?

Do not exceed recommended dosageFirmly insert extension tube into spray can valve and ensure it fits securely into the actuator openingposition the extension tube 1-2 inches from the affected area.Spray 1/2 second (press and immediately release the actuator)Anesthesia is accomplished in approximately 20 seconds.

Which are Opahl UNII Codes?

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

Which are Opahl 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 Opahl?

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".