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  4. NDC Product Code: 64762-871 Nbe

NDC 64762-871 Nbe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 64762-871?
  5. Nbe 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:
64762-871
Proprietary Name:
Nbe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dynamic Pharmaceuticals Inc.
Labeler Code:
64762
Product Label ID:
577ddfbf-13a1-490f-bcef-2f96cdf9ed28
Start Marketing Date: [9]
09-30-2010
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 64762-871?

The NDC code 64762-871 is assigned by the FDA to the product Nbe which is product labeled by Dynamic Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64762-871-30 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump. 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 Nbe?

For best results, use at the first sign of a cold and continue to use for an additional 48 hours after symptoms subside.Adults and children 3 years of age and older:Remove protective over-cap.Spray 4 - 5 times into mouth at the onset of symptoms.Spray on inside of cheeks, roof of mouth and gums. Retain for 15 seconds. Swallow.Repeat every three hours until symptoms are gone.To avoid minor stomach upset, do not take on an empty stomach.Do not eat or drink for 15 minutes after use. Do not eat or drink citrus fruits or juices for 30 minutes before or after use. Otherwise, drink plenty of fluids.Children under 3 years of age:Consult a doctor before use.

Which are Nbe UNII Codes?

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

Which are Nbe 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".