NDC 15821-108 Freshkote Preservative Free Lubricating Eye Drops
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 15821-108?
What are the uses for Freshkote Preservative Free Lubricating Eye Drops?
Which are Freshkote Preservative Free Lubricating Eye Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE (UNII: FZ989GH94E)
- POVIDONE (UNII: FZ989GH94E) (Active Moiety)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (Active Moiety)
Which are Freshkote Preservative Free Lubricating 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:
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Freshkote Preservative Free Lubricating Eye Drops?
- RxCUI: 630977 - polyvinyl alcohol 2.7 % / povidone 2 % Ophthalmic Solution
- RxCUI: 630977 - polyvinyl alcohol 27 MG/ML / povidone 20 MG/ML Ophthalmic Solution
- RxCUI: 630981 - FreshKote 2.7 % / 2 % Ophthalmic Solution
- RxCUI: 630981 - polyvinyl alcohol 27 MG/ML / povidone 20 MG/ML Ophthalmic Solution [Freshkote]
- RxCUI: 630981 - Freshkote (polyvinyl alcohol 1.8 % / polyvinyl alcohol 0.9 % / povidone 2 % ) 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".