NDC 15821-101 Freshkote Lubricant Eye Drops
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 15821-101?
What are the uses for Freshkote Lubricant Eye Drops?
Which are Freshkote Lubricant Eye Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE K29/32 (UNII: 390RMW2PEQ)
- POVIDONE K29/32 (UNII: 390RMW2PEQ) (Active Moiety)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POLYVINYL ALCOHOL (UNII: 532B59J990) (Active Moiety)
Which are Freshkote 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:
- BORIC ACID (UNII: R57ZHV85D4)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POLIXETONIUM (UNII: EJT309W86C)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Freshkote Lubricant 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".