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  4. NDC Product Code: 67172-595 Clear Eyes Complete 7 Symptom Relief

NDC 67172-595 Clear Eyes Complete 7 Symptom Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67172-595?
  4. Clear Eyes Complete 7 Symptom Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67172-595
Proprietary Name:
Clear Eyes Complete 7 Symptom Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prestige Brands Holdings, Inc.
Labeler Code:
67172
Product Label ID:
9a1ce5e2-c3da-424d-b754-cf2de8c655e3
Start Marketing Date: [9]
03-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67172-595-01

Package Description: 1 BOTTLE, DROPPER in 1 BOX / 15 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 67172-595?

The NDC code 67172-595 is assigned by the FDA to the product Clear Eyes Complete 7 Symptom Relief which is product labeled by Prestige Brands Holdings, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67172-595-01 1 bottle, dropper in 1 box / 15 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 Clear Eyes Complete 7 Symptom Relief?

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Which are Clear Eyes Complete 7 Symptom Relief UNII Codes?

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

Which are Clear Eyes Complete 7 Symptom 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:

What is the NDC to RxNorm Crosswalk for Clear Eyes Complete 7 Symptom Relief?

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: 1053133 - hypromellose 0.2 % / naphazoline HCl 0.025 % / polysorbate 80 0.5 % / zinc sulfate 0.25 % Ophthalmic Solution
  • RxCUI: 1053133 - hypromellose 2 MG/ML / naphazoline hydrochloride 0.25 MG/ML / polysorbate 80 5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
  • RxCUI: 1053133 - hypromellose 0.2 % / naphazoline HCl 0.025 % / polysorbate 80 0.5 % / zinc sulfate 0.25 % Ophthalmic Drops
  • RxCUI: 1053133 - hypromellose 2 MG/ML / Naphazoline Hydrochloride 0.25 MG/ML / Polysorbate 80 5 MG/ML / ZnSO4 2.5 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".