NDC 82095-700 Ivizia Dry Eye
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82095 - Laboratoires Thea
- 82095-700 - Ivizia Dry Eye
Product Packages
NDC Code 82095-700-05
Package Description: 5 mL in 1 BOTTLE, DROPPER
NDC Code 82095-700-11
Package Description: 10 mL in 1 BOTTLE, DROPPER
NDC Code 82095-700-13
Package Description: 5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 82095-700?
What are the uses for Ivizia Dry Eye?
Which are Ivizia Dry Eye UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE (UNII: FZ989GH94E)
- POVIDONE (UNII: FZ989GH94E) (Active Moiety)
Which are Ivizia Dry Eye 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:
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TREHALOSE (UNII: B8WCK70T7I)
- TROMETHAMINE (UNII: 023C2WHX2V)
What is the NDC to RxNorm Crosswalk for Ivizia Dry Eye?
- RxCUI: 2570860 - povidone 0.5 % Ophthalmic Solution
- RxCUI: 2570860 - povidone 5 MG/ML Ophthalmic Solution
- RxCUI: 2586186 - iVIZIA 0.5 % Ophthalmic Solution
- RxCUI: 2586186 - povidone 5 MG/ML Ophthalmic Solution [iVizia]
- RxCUI: 2586186 - iVizia 0.5 % Ophthalmic Solution
* Please review the disclaimer below.
[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".