NDC 69803-100 Kovanaze
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69803-100?
What are the uses for Kovanaze?
Which are Kovanaze UNII Codes?
The UNII codes for the active ingredients in this product are:
- TETRACAINE HYDROCHLORIDE (UNII: 5NF5D4OPCI)
- TETRACAINE (UNII: 0619F35CGV) (Active Moiety)
- OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY)
- OXYMETAZOLINE (UNII: 8VLN5B44ZY) (Active Moiety)
Which are Kovanaze 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Kovanaze?
- RxCUI: 1809050 - oxymetazoline HCl 0.1 MG / tetracaine HCl 6 MG per 0.2 ML Metered Dose Nasal Spray
- RxCUI: 1809050 - oxymetazoline hydrochloride 0.1 MG/ACTUAT / tetracaine hydrochloride 6 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1809050 - oxymetazoline hydrochloride 0.1 MG / tetracaine hydrochloride 6 MG per 0.2 ML Metered Dose Nasal Spray
- RxCUI: 1809050 - oxymetazoline hydrochloride 0.5 MG/ML / tetracaine hydrochloride 30 MG/ML Metered Dose Nasal Spray
- RxCUI: 1809056 - KOVANAZE 0.1 MG / 6 MG in 0.2 ML Metered Dose Nasal Spray
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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".