NDC 0065-0096 Flarex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0065 - Alcon Laboratories, Inc.
- 0065-0096 - Flarex
Product Packages
NDC Code 0065-0096-05
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Price per Unit: $24.00675 per ML
Product Details
What is NDC 0065-0096?
What are the uses for Flarex?
Which are Flarex UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUOROMETHOLONE ACETATE (UNII: 9I50C3I3OK)
- FLUOROMETHOLONE (UNII: SV0CSG527L) (Active Moiety)
Which are Flarex 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- TYLOXAPOL (UNII: Y27PUL9H56)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Flarex?
- RxCUI: 1249629 - fluorometholone acetate 0.1 % Ophthalmic Suspension
- RxCUI: 1249629 - fluorometholone acetate 1 MG/ML Ophthalmic Suspension
- RxCUI: 1249631 - Flarex 0.1 % Ophthalmic Suspension
- RxCUI: 1249631 - fluorometholone acetate 1 MG/ML Ophthalmic Suspension [Flarex]
- RxCUI: 1249631 - Flarex 1 MG/ML Ophthalmic Suspension
* 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".