NDC 0363-7746 Walgreens Artifical Tears Free

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:
0363-7746
Proprietary Name:
Walgreens Artifical Tears Free
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
0363
Start Marketing Date: [9]
07-16-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 0363-7746?

The NDC code 0363-7746 is assigned by the FDA to the product Walgreens Artifical Tears Free which is product labeled by Walgreens. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-7746-32 32 vial, single-dose in 1 carton / .6 ml in 1 vial, single-dose. 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 Walgreens Artifical Tears Free?

For the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun.For use as a protectant against further irritation or to relieve dryness of the eye.

Which are Walgreens Artifical Tears Free UNII Codes?

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

Which are Walgreens Artifical Tears Free 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 Walgreens Artifical Tears Free?

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: 309714 - dextran 70 0.1 % / hypromellose 0.3 % Ophthalmic Solution
  • RxCUI: 309714 - dextran 70 1 MG/ML / hypromellose 3 MG/ML Ophthalmic Solution
  • RxCUI: 309714 - dextran 70 0.1 % / hypromellose 0.3 % Ophthalmic Drops

* 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".