NDC 52389-172 Nauzene
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52389 - Alva-amco Pharmacal Companies, Inc.
- 52389-172 - Nauzene
Product Characteristics
Product Packages
NDC Code 52389-172-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52389-172?
What are the uses for Nauzene?
Which are Nauzene UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- DEXTROSE (UNII: IY9XDZ35W2)
- DEXTROSE (UNII: IY9XDZ35W2) (Active Moiety)
- FRUCTOSE (UNII: 6YSS42VSEV)
- FRUCTOSE (UNII: 6YSS42VSEV) (Active Moiety)
Which are Nauzene 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:
- CORN SYRUP (UNII: 9G5L16BK6N)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Nauzene?
- RxCUI: 895045 - glucose 4.35 GM / fructose 4.17 GM / sodium citrate 0.921 GM in 15 mL Oral Solution
- RxCUI: 895045 - fructose 278 MG/ML / glucose 290 MG/ML / sodium citrate 61.4 MG/ML Oral Solution
- RxCUI: 895045 - fructose 4.17 GM / glucose 4.35 GM / sodium citrate 0.921 GM per 15 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".