NDC 54868-6115 Xyzal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6115 - Xyzal
Product Characteristics
Product Packages
NDC Code 54868-6115-0
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 148 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 54868-6115?
What are the uses for Xyzal?
Which are Xyzal UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
- LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)
Which are Xyzal 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- ACETIC ACID (UNII: Q40Q9N063P)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Xyzal?
- RxCUI: 855168 - levocetirizine dihydrochloride 2.5 MG in 5 mL Oral Solution
- RxCUI: 855168 - levocetirizine dihydrochloride 0.5 MG/ML Oral Solution
- RxCUI: 855168 - levocetirizine dihydrochloride 2.5 MG per 5 ML Oral Solution
- RxCUI: 855170 - XYZAL 2.5 MG in 5 mL 24HR Oral Solution
- RxCUI: 855170 - levocetirizine dihydrochloride 0.5 MG/ML Oral Solution [Xyzal]
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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".