NDC 37205-138 Leader Relief Eye

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:
37205-138
Proprietary Name:
Leader Relief Eye
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Start Marketing Date: [9]
01-04-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37205-138-05

Package Description: 1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE

Price per Unit: $0.09707 per ML

Product Details

What is NDC 37205-138?

The NDC code 37205-138 is assigned by the FDA to the product Leader Relief Eye which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-138-05 1 bottle in 1 carton / 15 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 Leader Relief Eye?

Directionsinstill 1 or 2 drops in the affected eye(s) up to 4 times daily. Store at room temperature. Children under 6 years of age: Ask a doctor

Which are Leader Relief Eye UNII Codes?

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

Which are Leader Relief 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:

What is the NDC to RxNorm Crosswalk for Leader Relief Eye?

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: 1043249 - tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
  • RxCUI: 1043249 - tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
  • RxCUI: 1043249 - Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution

* Please review the disclaimer below.

Patient Education

Tetrahydrozoline Ophthalmic


Ophthalmic tetrahydrozoline is used to relieve minor eye irritation and redness caused by colds, pollen, and swimming.
[Learn More]


* 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".