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  4. NDC Product Code: 59262-348 Irritated Eye Relief

NDC 59262-348 Irritated Eye Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59262-348?
  4. Irritated Eye Relief 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:
59262-348
Proprietary Name:
Irritated Eye Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Similasan Corporation
Labeler Code:
59262
Product Label ID:
d21830b0-7e9d-48df-9905-8058774c55ed
Start Marketing Date: [9]
07-02-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59262-348-11

Package Description: 10 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 59262-348?

The NDC code 59262-348 is assigned by the FDA to the product Irritated Eye Relief which is product labeled by Similasan Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59262-348-11 10 ml in 1 bottle, dropper . 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 Irritated Eye Relief?

For adults and children ages 2 and over:remove tamper-evident seal from neck of bottle twist cap off bottle squeeze plastic tip to release 2-3 drops into eye apply as needed replace cap after use

Which are Irritated Eye Relief UNII Codes?

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

Which are Irritated Eye Relief 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".