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NDC 17312-024 Pink Eye

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 17312-024?
  4. Pink Eye 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:
17312-024
Proprietary Name:
Pink Eye
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Trp Company
Labeler Code:
17312
Product Label ID:
9800cae0-d58b-4890-8fe9-97f0ced63faa
Start Marketing Date: [9]
09-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 17312-024?

The NDC code 17312-024 is assigned by the FDA to the product Pink Eye which is product labeled by Trp Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 17312-024-11 1 bottle, dropper in 1 package / 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 Pink Eye?

For adults and children age 2 and over. Squeeze 1-3 drops in the eye. Use several times per day as needed. • Use within 30 days of opening. Expiration date only refers to unopened bottle.

Which are Pink Eye UNII Codes?

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

Which are Pink Eye 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".