NDC 21695-875 Oxymetazoline Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-875 - Oxymetazoline Hydrochloride
Product Packages
NDC Code 21695-875-15
Package Description: 15 mL in 1 BOTTLE, SPRAY
NDC Code 21695-875-30
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 21695-875?
What are the uses for Oxymetazoline Hydrochloride?
Which are Oxymetazoline Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY)
- OXYMETAZOLINE (UNII: 8VLN5B44ZY) (Active Moiety)
Which are Oxymetazoline Hydrochloride 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 PHOSPHATE, DIBASIC ANHYDROUS (UNII: 22ADO53M6F)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Oxymetazoline Hydrochloride?
- RxCUI: 1000990 - oxymetazoline HCl 0.05 % Nasal Spray
- RxCUI: 1000990 - oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray
- RxCUI: 1000990 - oxymetazoline hydrochloride 0.05 % Nasal Spray
* 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".