NDC 21695-969 Ciprodex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-969 - Ciprodex
Product Packages
NDC Code 21695-969-75
Package Description: 7.5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 21695-969?
What are the uses for Ciprodex?
Which are Ciprodex UNII Codes?
The UNII codes for the active ingredients in this product are:
- CIPROFLOXACIN HYDROCHLORIDE (UNII: 4BA73M5E37)
- CIPROFLOXACIN (UNII: 5E8K9I0O4U) (Active Moiety)
- DEXAMETHASONE (UNII: 7S5I7G3JQL)
- DEXAMETHASONE (UNII: 7S5I7G3JQL) (Active Moiety)
Which are Ciprodex 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)
- BORIC ACID (UNII: R57ZHV85D4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TYLOXAPOL (UNII: Y27PUL9H56)
- ACETIC ACID (UNII: Q40Q9N063P)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Ciprodex?
- RxCUI: 403908 - ciprofloxacin 0.3 % / dexAMETHasone 0.1 % Otic Suspension
- RxCUI: 403908 - ciprofloxacin 3 MG/ML / dexamethasone 1 MG/ML Otic Suspension
- RxCUI: 403908 - ciprofloxacin (as ciprofloxacin hydrochloride) 3 MG/ML / dexamethasone 1 MG/ML Otic Suspension
- RxCUI: 403908 - ciprofloxacin 0.3 % / dexamethasone 0.1 % Otic Suspension
- RxCUI: 404630 - CIPRODEX 0.3 % / 0.1 % Otic 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".