NDC 52389-172 Nauzene

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52389-172
Proprietary Name:
Nauzene
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Alva-amco Pharmacal Companies, Inc.
Labeler Code:
52389
Start Marketing Date: [9]
02-15-2000
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - FLAVOR)

Product Packages

NDC Code 52389-172-04

Package Description: 118 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 52389-172?

The NDC code 52389-172 is assigned by the FDA to the product Nauzene which is product labeled by Alva-amco Pharmacal Companies, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52389-172-04 118 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Nauzene?

Read all package directions and warnings before use and use only as directed.Adults:  1 - 2 tablespoons (15 - 30 mL).Children:  Consult a doctor for appropriate dosage.Dosage may be repeated after 30 minutes not to exceed 6 doses in a 24-hour period unless advised by a doctor.For maximum effectiveness never dilute Nauzene or drink fluids of any kind immediately before or after taking Nauzene.Nauzene Liquid is intended for use by normally healthy persons only.Persons under 18 years of age should use only as directed by a doctor.

Which are Nauzene UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Nauzene?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[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".