NDC 53807-422 Childrens Uniphed Nasal Decongestant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53807 - Rij Pharmaceutical Corporation
- 53807-422 - Childrens Uniphed
Product Characteristics
Product Packages
NDC Code 53807-422-04
Package Description: 118 mL in 1 BOTTLE
Product Details
What is NDC 53807-422?
What are the uses for Childrens Uniphed Nasal Decongestant?
Which are Childrens Uniphed Nasal Decongestant UNII Codes?
The UNII codes for the active ingredients in this product are:
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
Which are Childrens Uniphed 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Childrens Uniphed Nasal Decongestant?
- RxCUI: 1049143 - pseudoephedrine HCl 15 MG in 5 mL Oral Solution
- RxCUI: 1049143 - pseudoephedrine hydrochloride 3 MG/ML Oral Solution
- RxCUI: 1049143 - pseudoephedrine hydrochloride 15 MG per 5 ML Oral Solution
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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".