NDC 67510-0669 Nasal Decongestant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67510 - Kareway Product, Inc.
- 67510-0669 - Nasal Decongestant
Product Packages
NDC Code 67510-0669-1
Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE
Product Details
What is NDC 67510-0669?
What are the uses for Nasal Decongestant?
Which are Nasal Decongestant UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY)
- OXYMETAZOLINE (UNII: 8VLN5B44ZY) (Active Moiety)
Which are Nasal Decongestant 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)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Nasal Decongestant?
- 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
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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".