NDC 64048-5000 Nasal Decongestant Rhinall
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What is NDC 64048-5000?
What are the uses for Nasal Decongestant Rhinall?
Which are Nasal Decongestant Rhinall UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Nasal Decongestant Rhinall 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)
- CHLOROBUTANOL HEMIHYDRATE (UNII: 3X4P6271OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Nasal Decongestant Rhinall?
- RxCUI: 1234576 - phenylephrine HCl 0.25 % Nasal Spray
- RxCUI: 1234576 - phenylephrine hydrochloride 2.5 MG/ML Nasal Spray
- RxCUI: 1234576 - phenylephrine hydrochloride 0.25 % 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".