NDC 20146-7000 Pure Eyes Sterile Eyes

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
20146-7000
Proprietary Name:
Pure Eyes Sterile Eyes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Samson Pharmaceutical
Labeler Code:
20146
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 20146-7000-1

Package Description: 1 BOTTLE in 1 BLISTER PACK / 7 mL in 1 BOTTLE

Product Details

What is NDC 20146-7000?

The NDC code 20146-7000 is assigned by the FDA to the product Pure Eyes Sterile Eyes which is product labeled by Samson Pharmaceutical. The product's dosage form is . The product is distributed in a single package with assigned NDC code 20146-7000-1 1 bottle in 1 blister pack / 7 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 Pure Eyes Sterile Eyes?

♦Instill 1 to 2 drops in the affected eye(s) up to 4 times daily

Which are Pure Eyes Sterile Eyes UNII Codes?

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

Which are Pure Eyes Sterile Eyes 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:

What is the NDC to RxNorm Crosswalk for Pure Eyes Sterile Eyes?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1046700 - glycerin 0.25 % / naphazoline HCl 0.012 % Ophthalmic Solution
  • RxCUI: 1046700 - glycerin 2.5 MG/ML / naphazoline hydrochloride 0.12 MG/ML Ophthalmic Solution

* 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".