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  4. NDC Product Code: 61508-0166 60 Second Gel Mint

NDC 61508-0166 60 Second Gel Mint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61508-0166?
  5. 60 Second Gel Mint Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61508-0166
Proprietary Name:
60 Second Gel Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Germiphene Corporation
Labeler Code:
61508
Product Label ID:
487f6aa0-be7d-39f8-e054-00144ff88e88
Start Marketing Date: [9]
02-24-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
BUBBLE GUM (C73368)
STRAWBERRY (C73417)
GRAPE (C73391)
MINT (C73404)

Code Structure Chart

Product Details

What is NDC 61508-0166?

The NDC code 61508-0166 is assigned by the FDA to the product 60 Second Gel Mint which is product labeled by Germiphene Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61508-0166-1 450 g in 1 bottle, plastic . 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 60 Second Gel Mint?

Shake well before using. Fill Germiphene brand disposable trays to appropriate level. After prophylaxis, air dry teeth and insert trays for one minute. Remove trays and have patient expectorate excess gel.

Which are 60 Second Gel Mint UNII Codes?

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

Which are 60 Second Gel Mint 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:

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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".