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  4. NDC Product Code: 43913-402 G-bucal-c

NDC 43913-402 G-bucal-c

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 43913-402?
  5. G-bucal-c 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:
43913-402
Proprietary Name:
G-bucal-c
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mclaren Medical Inc
Labeler Code:
43913
Product Label ID:
31690548-0a55-4d72-8733-591ba3a9be92
Start Marketing Date: [9]
01-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
PEPPERMINT (C73408)

Code Structure Chart

Product Details

What is NDC 43913-402?

The NDC code 43913-402 is assigned by the FDA to the product G-bucal-c which is product labeled by Mclaren Medical Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43913-402-30 30 ml in 1 bottle, spray . 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 G-bucal-c?

For the temporary relief of occasional minor throat irritation, pain, sore mouth, sore throat, pain associated with canker sores, pain due to minor irritation or injury of the mouth and gums, pain due to minor dental procedures, pain due to minor irritations caused by dentures or orthodontic appliance, sore gums due to teething in infants and children 4 months of age and older.

Which are G-bucal-c UNII Codes?

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

Which are G-bucal-c 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 G-bucal-c?

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: 1291083 - benzocaine 2 % / cetylpyridinium Cl 0.1 % / menthol 0.15 % / zinc chloride 0.1 % Mucosal Spray
  • RxCUI: 1291083 - benzocaine 20 MG/ML / cetylpyridinium chloride 1 MG/ML / menthol 1.5 MG/ML / zinc chloride 1 MG/ML Mucosal Spray
  • RxCUI: 1291083 - benzocaine 2 % / cetylpyridinium Cl 0.1 % / menthol 1.5 % / zinc chloride 0.1 % Mucosal Spray

* 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".