NDC 59276-905 Lubricant Eye Drops

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:
59276-905
Proprietary Name:
Lubricant Eye Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
59276
Start Marketing Date: [9]
02-25-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 59276-905?

The NDC code 59276-905 is assigned by the FDA to the product Lubricant Eye Drops which is product labeled by Oliver Landon Intl Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59276-905-05 5 vial, single-use in 1 cello pack / .4 ml in 1 vial, single-use. 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 Lubricant Eye Drops?

•To open, TWIST AND PULL TAB TO REMOVE. •Instill 1 or 2 drops in the affected eye(s) as needed and discard container.*If used for post-operative dryness and discomfort, follow your eye doctor’s instructions.

Which are Lubricant Eye Drops UNII Codes?

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

  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)

Which are Lubricant Eye Drops 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 Lubricant Eye Drops?

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: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 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".