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  4. NDC Product Code: 57483-003 Ejectdelay Gel

NDC 57483-003 Ejectdelay Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57483-003?
  4. Ejectdelay Gel 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:
57483-003
Proprietary Name:
Ejectdelay Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Innovus Pharmaceuticals, Inc.
Labeler Code:
57483
Product Label ID:
24a9e4e5-a418-43a2-890f-7f90cd5f5b3f
Start Marketing Date: [9]
07-15-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 57483-003-07

Package Description: 1 TUBE in 1 BOX / 56.8 g in 1 TUBE (57483-003-03)

NDC Code 57483-003-08

Package Description: 5 g in 1 PACKET

Product Details

What is NDC 57483-003?

The NDC code 57483-003 is assigned by the FDA to the product Ejectdelay Gel which is product labeled by Innovus Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 57483-003-07 1 tube in 1 box / 56.8 g in 1 tube (57483-003-03), 57483-003-08 5 g in 1 packet . 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 Ejectdelay Gel?

Helps in the prevention of premature ejaculation

Which are Ejectdelay Gel UNII Codes?

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

Which are Ejectdelay Gel 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".