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  4. NDC Product Code: 72151-602 Pepteron

NDC 72151-602 Pepteron

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72151-602?
  4. Pepteron Uses
  5. Active Ingredients UNII Codes
  6. 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:
72151-602
Proprietary Name:
Pepteron
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Maitland Labs Of Central Florida
Labeler Code:
72151
Product Label ID:
003f4fa6-c3b6-486f-a4e1-29100ad3c083
Start Marketing Date: [9]
03-26-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72151-602-05

Package Description: 5 mL in 1 BOTTLE

Product Details

What is NDC 72151-602?

The NDC code 72151-602 is assigned by the FDA to the product Pepteron which is product labeled by Maitland Labs Of Central Florida. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72151-602-05 5 ml 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 Pepteron?

•   Do not use if tamperproof cover is missing•   Press down 4 times to prime the pump.spray once in to each nostril.Use 2 times per day to relieve discomfort.

Which are Pepteron UNII Codes?

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

Which are Pepteron 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:

* 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".