1. Home
  2. Labeler Index
  3. Zenith Medicosm Sl
  4. NDC Product Code: 42248-127 Protector R Plus

NDC 42248-127 Protector R Plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42248-127?
  4. Active Ingredients UNII Codes
  5. 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:
42248-127
Proprietary Name:
Protector R Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zenith Medicosm Sl
Labeler Code:
42248
Product Label ID:
72ac1954-f94e-494c-99cd-3c70a321e45f
Start Marketing Date: [9]
12-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42248-127-02

Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE

Product Details

What is NDC 42248-127?

The NDC code 42248-127 is assigned by the FDA to the product Protector R Plus which is product labeled by Zenith Medicosm Sl. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42248-127-02 1 tube in 1 box / 50 ml in 1 tube. 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.

Which are Protector R Plus UNII Codes?

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

Which are Protector R Plus 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".