NDC 54868-2032 Hydroxyzine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2032 - Hydroxyzine Hydrochloride
Product Packages
NDC Code 54868-2032-0
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-2032?
What are the uses for Hydroxyzine Hydrochloride?
Which are Hydroxyzine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROXYZINE HYDROCHLORIDE (UNII: 76755771U3)
- HYDROXYZINE (UNII: 30S50YM8OG) (Active Moiety)
Which are Hydroxyzine 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:
- ALCOHOL (UNII: 3K9958V90M)
- CORN SYRUP (UNII: 9G5L16BK6N)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PEPPERMINT (UNII: V95R5KMY2B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Hydroxyzine Hydrochloride?
- RxCUI: 995241 - hydrOXYzine HCl 10 MG in 5 mL Oral Solution
- RxCUI: 995241 - hydroxyzine hydrochloride 2 MG/ML Oral Solution
- RxCUI: 995241 - hydroxyzine hydrochloride 10 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".