NDC 64809-104 Eyesaline Concentrate

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:
64809-104
Proprietary Name:
Eyesaline Concentrate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
64809
Start Marketing Date: [9]
09-08-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 64809-104?

The NDC code 64809-104 is assigned by the FDA to the product Eyesaline Concentrate which is product labeled by Sperian Eye & Face Protection Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 64809-104-18 2070 ml in 1 bottle, plastic , 64809-104-19 5323 ml in 1 bottle, plastic . 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 Eyesaline Concentrate?

Concentrate must be diluted (1) part concentrate to (10) parts potable water before usePrepare sufficient quantity of constituted eyewash solution in advance of an emergencyMix concentrate with potable water to prepare eyewash solution as follows:Determine quantity of eyewash solution requiredFollow sanitary proceduresWear protective eyewear and glovesPour 1/3 of required amount of potable water into mixing container or eyewash unitAdd 1/3 of required amount of concentrate to waterAgitate or mix thoroughly​Repeat until required amount of solution is preparedProperly dispose of empty bottle after useDo not reuse.Replace solution no longer than (6) months after mixing

Which are Eyesaline Concentrate UNII Codes?

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

Which are Eyesaline Concentrate 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 Eyesaline Concentrate?

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: 1150133 - water 92.2 % Concentrate for Ophthalmic Irrigation Solution
  • RxCUI: 1150133 - water 922 MG/ML Ophthalmic Irrigation Solution

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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".