NDC 73450-002 Lubricant Eye Drops Preservative Free 30 Single Use Container
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73450 - Nexus Optical Inc
- 73450-002 - Lubricant Eye Drops Preservative Free 30 Single Use Container
Product Packages
NDC Code 73450-002-05
Package Description: 30 VIAL, SINGLE-USE in 1 BOX / .5 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 73450-002?
What are the uses for Lubricant Eye Drops Preservative Free 30 Single Use Container?
Which are Lubricant Eye Drops Preservative Free 30 Single Use Container 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 Preservative Free 30 Single Use Container 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:
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
What is the NDC to RxNorm Crosswalk for Lubricant Eye Drops Preservative Free 30 Single Use Container?
- 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
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[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".